FDA Recalled Drugs


Heparin Sodium

Recalling Firm: Hospira Inc.

Recall Initiation Date: Thursday September 11th, 2014

Reason for Recall: Presence of Particulate Matter: A particulate, confirmed as human hair, was found sealed between the tube and film at the round seal of the unused administrative port of the container.


http://dailymed.nlm.nih.gov/dailymed/image.cfm?setid=57517a0e-ec1b-4605-a7cc-7e3801158ec9&name=cefepime-for-injection-in-duplex-7.jpg

Cefepime Hydrochloride And Dextrose

Recalling Firm: B. Braun Medical Inc

Recall Initiation Date: Thursday November 21st, 2013

Reason for Recall: Presence of Particulate Matter: B. Braun Medical Inc. is recalling several injectable products due to visible particulate matter found in reserve sample units.


Venlafaxine Hydrochloride

Recalling Firm: Greenstone Llc

Recall Initiation Date: Thursday March 6th, 2014

Reason for Recall: Presence of Foreign Tablets/Capsules: A Pharmacist reported a foreign capsule with markings (TKN 250) and identified as a Tikosyn (dofetilide) capsule in a lot of Effexor XR 150 mg capsules that was packaged in the same packaging campaign as this Venlafaxine HCl lot.


http://dailymed.nlm.nih.gov/dailymed/image.cfm?setid=53351231-eade-4a20-bf1e-552a5b1a8faf&name=MM4.jpg

Venlafaxine Hydrochloride

Recalling Firm: Greenstone Llc

Recall Initiation Date: Thursday March 6th, 2014

Reason for Recall: Presence of Foreign Tablets/Capsules: A Pharmacist reported a foreign capsule with markings (TKN 250) and identified as a Tikosyn (dofetilide) capsule in a lot of Effexor XR 150 mg capsules that was packaged in the same packaging campaign as this Venlafaxine HCl lot.


Procalamine

Recalling Firm: B. Braun Medical Inc

Recall Initiation Date: Thursday November 21st, 2013

Reason for Recall: Presence of Particulate Matter: B. Braun Medical Inc. is recalling several injectable products due to visible particulate matter found in reserve sample units.


http://dailymed.nlm.nih.gov/dailymed/image.cfm?setid=cc14fafd-3dcd-4fc8-bdbd-6f355c375768&name=sodium-chloride-injection-usp-in-pab-5.jpg

Sodium Chloride

Recalling Firm: B. Braun Medical Inc

Recall Initiation Date: Thursday November 21st, 2013

Reason for Recall: Presence of Particulate Matter: B. Braun Medical Inc. is recalling several injectable products due to visible particulate matter found in reserve sample units.


http://dailymed.nlm.nih.gov/dailymed/image.cfm?setid=517d10ba-08ce-4410-d594-5618a48866c9&name=aminosyn-ii1-figure-2-JIM-0634.jpg

Aminosyn Ii

Recalling Firm: Hospira Inc.

Recall Initiation Date: Friday August 30th, 2013

Reason for Recall: Presence of Particulate Matter: Confirmed customer complaint of particulate matter, identified as a human hair, visible in the injection port and primary container.


http://dailymed.nlm.nih.gov/dailymed/image.cfm?setid=6ea7ec73-403e-4303-8862-6380e2f1fda6&name=freamine-hbc-in-glass-3.jpg

Freamine Hbc

Recalling Firm: B. Braun Medical Inc

Recall Initiation Date: Thursday November 21st, 2013

Reason for Recall: Presence of Particulate Matter: B. Braun Medical Inc. is recalling several injectable products due to visible particulate matter found in reserve sample units.


http://dailymed.nlm.nih.gov/dailymed/image.cfm?setid=4b163d1c-0bd6-4002-a954-b1b2cc8325bc&name=metformin-hcl-er-500mg-for-amneal-2.jpg

Metformin Hydrochloride

Recalling Firm: Shamrock Medical Solutions Group LLC

Recall Initiation Date: Tuesday September 27th, 2011

Reason for Recall: Labeling: Label Mix up; product labeled did not indicated Extended Release


http://dailymed.nlm.nih.gov/dailymed/image.cfm?setid=93c8ceff-b70b-4a53-9c87-7c76e342e2c6&name=image-02.jpg

Pain Relief

Recalling Firm: Shamrock Medical Solutions Group LLC

Recall Initiation Date: Tuesday September 27th, 2011

Reason for Recall: Labeling: Label Mix up; product labeled did not indicated Extended Release


http://dailymed.nlm.nih.gov/dailymed/image.cfm?setid=ee2739df-8db4-4b05-9a81-1590efbb589b&name=metformin-hydrochloride-extended-release-tablets-u-2.jpg

Ibandronate Sodium

Recalling Firm: Shamrock Medical Solutions Group LLC

Recall Initiation Date: Tuesday September 27th, 2011

Reason for Recall: Labeling: Label Mix up; product labeled did not indicated Extended Release


http://dailymed.nlm.nih.gov/dailymed/image.cfm?setid=8469d6fb-d6ef-476f-8cc3-0905192de0a8&name=8469d6fb-d6ef-476f-8cc3-0905192de0a8-03.jpg

Clinimix E

Recalling Firm: Baxter Healthcare Corp.

Recall Initiation Date: Monday November 18th, 2013

Reason for Recall: Presence of Particulate Matter: Particulate matter includes wood, sodium citrate and dextrose.


http://dailymed.nlm.nih.gov/dailymed/image.cfm?setid=c0f238ff-2804-4150-9766-22a5111b4e74&name=coum-5mginj.jpg

Coumadin

Recalling Firm: Bristol-Meyers Squibb

Recall Initiation Date: Monday May 12th, 2014

Reason for Recall: Presence of Particulate Matter: particulate matter identified as metallic-like and non-metallic cellulose fiber particles found in retain vials


Atorvastatin Calcium

Recalling Firm: Shire Human Genetic Therapies, Inc.

Recall Initiation Date: Friday March 14th, 2014

Reason for Recall: Presence of Particulate Matter; Particulates identified as stainless steel and barium sulfate.


http://dailymed.nlm.nih.gov/dailymed/image.cfm?setid=457a026c-ebce-4701-9deb-2d7652759a99&name=image-03.jpg

Nitroglycerin In Dextrose

Recalling Firm: Baxter Healthcare Corp.

Recall Initiation Date: Monday November 18th, 2013

Reason for Recall: Presence of Particulate Matter; particulate matter in one vial identified as silicone rubber and EPDM rubber from the vial stopper.


Effexor Xr

Recalling Firm: Pfizer Us Pharmaceutical Group

Recall Initiation Date: Thursday March 6th, 2014

Reason for Recall: Presence of Foreign Tablets/Capsules: A Pharmacist reported that a bottle of Effexor XR 150 mg capsules contained a single peach colored capsule printed TKN250 which was identified as a Tikosyn (dofetilide) capsule.


http://dailymed.nlm.nih.gov/dailymed/image.cfm?setid=4fabbef0-1838-4f70-aaf9-9550bd5f6204&name=1f8f63a5-0e05-4643-8f9a-ee1292931451-04.jpg

Effexor Xr

Recalling Firm: Pfizer Us Pharmaceutical Group

Recall Initiation Date: Thursday March 6th, 2014

Reason for Recall: Presence of Foreign Tablets/Capsules: A Pharmacist reported that a bottle of Effexor XR 150 mg capsules contained a single peach colored capsule printed TKN250 which was identified as a Tikosyn (dofetilide) capsule.


http://dailymed.nlm.nih.gov/dailymed/image.cfm?setid=a0aedcb7-8bf6-4e2b-a85a-dd8f1411dcfc&name=plenamine-amino-acids-injection-in-glass-8.jpg

Amino Acids

Recalling Firm: B. Braun Medical Inc

Recall Initiation Date: Thursday November 21st, 2013

Reason for Recall: Presence of Particulate Matter: B. Braun Medical Inc. is recalling several injectable products due to visible particulate matter found in reserve sample units.


http://dailymed.nlm.nih.gov/dailymed/image.cfm?setid=dccff103-8695-400c-a15d-cc2fd078760a&name=0aa46f4c-e595-4301-bc42-c472d9cfe264-03.jpg

Clinimix

Recalling Firm: Baxter Healthcare Corp.

Recall Initiation Date: Monday November 18th, 2013

Reason for Recall: Presence of Particulate Matter: Particulate matter includes wood, sodium citrate and dextrose.


http://dailymed.nlm.nih.gov/dailymed/image.cfm?setid=dc537761-d5f4-488d-24ab-b2bcd2b17b7a&name=dobutamine-injection-usp2-figure-2-dobutamine-figure-2.jpg

Dobutamine Hydrochloride

Recalling Firm: Hospira Inc.

Recall Initiation Date: Friday January 10th, 2014

Reason for Recall: Presence of Particulate Matter: Discolored solution due to a chip in the glass at the neck of the vial, also glass particulate was found within the solution.


http://dailymed.nlm.nih.gov/dailymed/image.cfm?setid=1d88fbe0-eb97-4964-8a78-88940064f8f0&name=trophamine-in-glass-3.jpg

Trophamine

Recalling Firm: B. Braun Medical Inc

Recall Initiation Date: Thursday November 21st, 2013

Reason for Recall: Presence of Particulate Matter: B. Braun Medical Inc. is recalling several injectable products due to visible particulate matter found in reserve sample units.


http://dailymed.nlm.nih.gov/dailymed/image.cfm?setid=092ddee4-572d-4771-8d95-880cea01097e&name=33c0b37a-b236-4cd3-aa90-f14080aab9ff-01.jpg

Potassium Chloride

Recalling Firm: Baxter Healthcare Corp.

Recall Initiation Date: Friday July 11th, 2014

Reason for Recall: Presence of Particulate Matter: particulate matter identified as fibers and/or plastics.


http://dailymed.nlm.nih.gov/dailymed/image.cfm?setid=6c7e9485-1ede-411c-8c46-911439332864&name=cefoxitin-for-injection-and-dextrose-injection-in--10.jpg

Cefoxitin And Dextrose

Recalling Firm: B. Braun Medical Inc

Recall Initiation Date: Thursday November 21st, 2013

Reason for Recall: Presence of Particulate Matter: B. Braun Medical Inc. is recalling several injectable products due to visible particulate matter found in reserve sample units.


http://dailymed.nlm.nih.gov/dailymed/image.cfm?setid=8fd7b5d8-f6b1-4d0a-9ec6-446c5f89762a&name=5670.jpg

Acetylcysteine Solution

Recalling Firm: Ben Venue Laboratories Inc

Recall Initiation Date: Friday February 14th, 2014

Reason for Recall: Presence of Particulate Matter: During a review of retain samples, the firm found a glass particulate in one lot of Acetylcysteine Solution


http://dailymed.nlm.nih.gov/dailymed/image.cfm?setid=46908d72-4675-4b43-b0f0-a972c3c76988&name=75406bd9-25e8-4696-8cd7-20fef714d887-03.jpg

Acetylcysteine Solution

Recalling Firm: Ben Venue Laboratories Inc

Recall Initiation Date: Friday February 14th, 2014

Reason for Recall: Presence of Particulate Matter: During a review of retain samples, the firm found a glass particulate in one lot of Acetylcysteine Solution


http://dailymed.nlm.nih.gov/dailymed/image.cfm?setid=829e3bd1-fb1c-4613-9db3-9a89ef8e2c0c&name=mlk02-0000-05.jpg

Mlk F4 Kit

Recalling Firm: Hospira Inc.

Recall Initiation Date: Friday October 18th, 2013

Reason for Recall: Presence of Particulate Matter: Units of this lot may have visible metal particles embedded in the vial and in the solution causing the product to be discolored.


http://dailymed.nlm.nih.gov/dailymed/image.cfm?setid=1c157964-1977-4617-9f01-76ca01fb0f8f&name=mar07-0000-05.jpg

Marbeta 25 Kit

Recalling Firm: Hospira Inc.

Recall Initiation Date: Friday October 18th, 2013

Reason for Recall: Presence of Particulate Matter: Units of this lot may have visible metal particles embedded in the vial and in the solution causing the product to be discolored.


http://dailymed.nlm.nih.gov/dailymed/image.cfm?setid=8978a093-289a-42ce-b266-6b71502420cc&name=MM2.jpg

Marcaine

Recalling Firm: Hospira Inc.

Recall Initiation Date: Friday October 18th, 2013

Reason for Recall: Presence of Particulate Matter: Units of this lot may have visible metal particles embedded in the vial and in the solution causing the product to be discolored.


http://dailymed.nlm.nih.gov/dailymed/image.cfm?setid=2295d3e9-4a14-482b-a6ef-35d6b7ca5f1b&name=MM2.jpg

Marcaine

Recalling Firm: Hospira Inc.

Recall Initiation Date: Friday October 18th, 2013

Reason for Recall: Presence of Particulate Matter: Units of this lot may have visible metal particles embedded in the vial and in the solution causing the product to be discolored.


http://dailymed.nlm.nih.gov/dailymed/image.cfm?setid=c6ea91fe-1f18-4c0f-81b5-cfd27f79adb8&name=1660-0.jpg

Marcaine

Recalling Firm: Hospira Inc.

Recall Initiation Date: Friday October 18th, 2013

Reason for Recall: Presence of Particulate Matter: Units of this lot may have visible metal particles embedded in the vial and in the solution causing the product to be discolored.


http://dailymed.nlm.nih.gov/dailymed/image.cfm?setid=0ab78381-8129-49d5-87ae-679bbc6a21c9&name=67d9feff-0cae-4c4c-bc45-f0b7aee7705c-03.jpg

Marcaine

Recalling Firm: Hospira Inc.

Recall Initiation Date: Friday October 18th, 2013

Reason for Recall: Presence of Particulate Matter: Units of this lot may have visible metal particles embedded in the vial and in the solution causing the product to be discolored.


http://dailymed.nlm.nih.gov/dailymed/image.cfm?setid=6a60cb55-530a-41ee-bc78-971eaf9f0850&name=3134.jpg

Marcaine

Recalling Firm: Hospira Inc.

Recall Initiation Date: Friday October 18th, 2013

Reason for Recall: Presence of Particulate Matter: Units of this lot may have visible metal particles embedded in the vial and in the solution causing the product to be discolored.


http://dailymed.nlm.nih.gov/dailymed/image.cfm?setid=67578b56-7540-487e-1fba-481255620e78&name=ca-3497.jpg

Marcaine

Recalling Firm: Hospira Inc.

Recall Initiation Date: Friday October 18th, 2013

Reason for Recall: Presence of Particulate Matter: Units of this lot may have visible metal particles embedded in the vial and in the solution causing the product to be discolored.


http://dailymed.nlm.nih.gov/dailymed/image.cfm?setid=ebcd67fa-b4d1-4a22-b33d-ee8bf6b9c722&name=soliris-1.jpg

Soliris

Recalling Firm: Alexion Pharmaceuticals, Inc.

Recall Initiation Date: Monday November 4th, 2013

Reason for Recall: Presence of Particulate Matter: Failed the appearance test for the presence of visible particles.


http://dailymed.nlm.nih.gov/dailymed/image.cfm?setid=beb5b6e0-46ed-443d-aad9-eebe389b7672&name=hyperlyte-cr-multi-electrolyte-concentrate-in-glas-3.jpg

Hyperlyte Cr

Recalling Firm: B. Braun Medical Inc

Recall Initiation Date: Thursday November 21st, 2013

Reason for Recall: Presence of Particulate Matter: B. Braun Medical Inc. is recalling several injectable products due to visible particulate matter found in reserve sample units.


Cefazolin Sodium Solution

Recalling Firm: B. Braun Medical Inc

Recall Initiation Date: Thursday November 21st, 2013

Reason for Recall: Presence of Particulate Matter: B. Braun Medical Inc. is recalling several injectable products due to visible particulate matter found in reserve sample units.


http://dailymed.nlm.nih.gov/dailymed/image.cfm?setid=089fc1de-00ae-41b6-7c97-1217f0cecc03&name=sodium-chloride-injection-usp5-figure-1-jIM-0092.jpg

Sodium Chloride

Recalling Firm: Hospira Inc.

Recall Initiation Date: Tuesday January 20th, 2015

Reason for Recall: Presence of Particulate Matter; Hospira has identified the particulate as a human hair, sealed in the bag at the additive port area.


http://dailymed.nlm.nih.gov/dailymed/image.cfm?setid=7699dd48-068e-4f74-bb50-c0f6cc531263&name=Label1.jpg

Propofol

Recalling Firm: Hospira Inc.

Recall Initiation Date: Monday October 6th, 2014

Reason for Recall: Temperature Abuse: Products experienced uncontrolled temperature excursions during transit.


http://dailymed.nlm.nih.gov/dailymed/image.cfm?setid=28d7ba00-f824-4e55-139a-03f509c099db&name=CartonNDC0409-4699-30Back.jpg

Propofol

Recalling Firm: Hospira Inc.

Recall Initiation Date: Monday October 6th, 2014

Reason for Recall: Temperature Abuse: Products experienced uncontrolled temperature excursions during transit.


http://dailymed.nlm.nih.gov/dailymed/image.cfm?setid=dad7735c-709b-40ea-ab7a-15577e24a966&name=89be82de-4d68-4449-8da5-21e5dda26d13-01.jpg

Lactated Ringers

Recalling Firm: Baxter Healthcare Corp.

Recall Initiation Date: Tuesday March 24th, 2015

Reason for Recall: Presence of Particulate Matter: Products recalled due to presence of particulate matter (metal)


http://dailymed.nlm.nih.gov/dailymed/image.cfm?setid=ef5e1735-9517-4736-8703-5c69610f49b2&name=MM1.jpg

Lactated Ringers

Recalling Firm: Baxter Healthcare Corp.

Recall Initiation Date: Tuesday March 24th, 2015

Reason for Recall: Presence of Particulate Matter: Products recalled due to presence of particulate matter (metal)


http://dailymed.nlm.nih.gov/dailymed/image.cfm?setid=4c778977-aaa1-4da2-93c6-c5ed7d32d87a&name=mucinex-01.jpg

Mucinex Fast-max Cold And Sinus

Recalling Firm: Reckitt Benckiser LLC

Recall Initiation Date: Wednesday April 15th, 2015

Reason for Recall: Labeling: Label Mix-Up; Bottles of Mucinex Fast-Max liquid are correctly labeled on the front of the label, however the back of the bottle where the Drug Facts labeling is, is missing certain Active Ingredients such as acetaminophen, phenylephrine, dextromethorphan, diphenhydramine, and/or guaifenesin. As a result certain safety warnings associated with those ingredients may also be missing.


http://dailymed.nlm.nih.gov/dailymed/image.cfm?setid=19228ba2-098d-47d0-9029-804b4627f98d&name=mucinex-01.jpg

Mucinex Fast-max Day Time Severe Cold And Mucinex Fast-max Night Time Cold And Flu Maximum Strength

Recalling Firm: Reckitt Benckiser LLC

Recall Initiation Date: Wednesday April 15th, 2015

Reason for Recall: Labeling: Label Mix-Up; Bottles of Mucinex Fast-Max liquid are correctly labeled on the front of the label, however the back of the bottle where the Drug Facts labeling is, is missing certain Active Ingredients such as acetaminophen, phenylephrine, dextromethorphan, diphenhydramine, and/or guaifenesin. As a result certain safety warnings associated with those ingredients may also be missing.


http://dailymed.nlm.nih.gov/dailymed/image.cfm?setid=90bda715-70d4-44a2-5ba8-13c8467855a5&name=lactated-ringers-irrigation1-figure-2-JIM-0198.jpg

Lactated Ringers

Recalling Firm: Hospira Inc.

Recall Initiation Date: Wednesday March 11th, 2015

Reason for Recall: Non-Sterility: Confirmed customer report of dark, fibrous particulates floating within the solution of the primary container, which were subsequently identified as mold


http://dailymed.nlm.nih.gov/dailymed/image.cfm?setid=fd683410-ed74-4309-bebb-acf9bdcfe336&name=image-01.jpg

Bupivacaine Hydrochloride And Epinephrine

Recalling Firm: Hospira Inc.

Recall Initiation Date: Thursday April 23rd, 2015

Reason for Recall: Presence of Particulate Matter: Presence of free-floating and embedded iron oxide particles.


http://dailymed.nlm.nih.gov/dailymed/image.cfm?setid=ca22671e-4184-4f5b-b8c2-942768db693c&name=15922-20.jpg

15922-20 Continuous Epidural 18g Tuohy

Recalling Firm: Hospira Inc.

Recall Initiation Date: Thursday April 23rd, 2015

Reason for Recall: Presence of Particulate Matter: Presence of free-floating and embedded iron oxide particles.


http://dailymed.nlm.nih.gov/dailymed/image.cfm?setid=272f30af-1f4a-406b-a23a-0d955ed6a0bb&name=A3852-17-27.jpg

A3852-1727 Combined Spinalepidural 17g Tuohy

Recalling Firm: Hospira Inc.

Recall Initiation Date: Thursday April 23rd, 2015

Reason for Recall: Presence of Particulate Matter: Presence of free-floating and embedded iron oxide particles.


http://dailymed.nlm.nih.gov/dailymed/image.cfm?setid=3d0606f3-ee9f-42d8-a345-89c2d43d4ffb&name=image-02.jpg

Bupivacaine Hydrochloride

Recalling Firm: Hospira Inc.

Recall Initiation Date: Thursday April 23rd, 2015

Reason for Recall: Presence of Particulate Matter: Presence of free-floating and embedded iron oxide particles.


http://dailymed.nlm.nih.gov/dailymed/image.cfm?setid=02a845c3-4521-4926-e397-25ab536e7cf6&name=bupivacaine-hydrochloride-injection,-usp1-figure-16-jIM-0382.jpg

Atenolol

Recalling Firm: Hospira Inc.

Recall Initiation Date: Thursday April 23rd, 2015

Reason for Recall: Presence of Particulate Matter: Presence of free-floating and embedded iron oxide particles.


http://dailymed.nlm.nih.gov/dailymed/image.cfm?setid=67b6d8b9-5944-4961-894a-13d214cc3229&name=Label1.jpg

Bupivacaine Hydrochloride

Recalling Firm: Hospira Inc.

Recall Initiation Date: Thursday April 23rd, 2015

Reason for Recall: Presence of Particulate Matter: Presence of free-floating and embedded iron oxide particles.


http://dailymed.nlm.nih.gov/dailymed/image.cfm?setid=6e7fe2ee-5ee5-40a0-8644-9999032ac716&name=Label1.jpg

Bupivacaine Hydrochloride

Recalling Firm: Hospira Inc.

Recall Initiation Date: Thursday April 23rd, 2015

Reason for Recall: Presence of Particulate Matter: Presence of free-floating and embedded iron oxide particles.


http://dailymed.nlm.nih.gov/dailymed/image.cfm?setid=348f581d-eb63-44c3-8f67-c7eb47fdf170&name=ms-mucinex-01.jpg

Mucinex Fast-max Day Time Severe Congestion And Cough And Mucinex Fast-max Night Time Cold And Flu Maximum Strength

Recalling Firm: Reckitt Benckiser LLC

Recall Initiation Date: Wednesday April 15th, 2015

Reason for Recall: Labeling: Label Mix-Up; Bottles of Mucinex Fast-Max liquid are correctly labeled on the front of the label, however the back of the bottle where the Drug Facts labeling is, is missing certain Active Ingredients such as acetaminophen, phenylephrine, dextromethorphan, diphenhydramine, and/or guaifenesin. As a result certain safety warnings associated with those ingredients may also be missing.


http://dailymed.nlm.nih.gov/dailymed/image.cfm?setid=03ebeabb-8386-4af4-3086-bdf3c3fc4a5a&name=magnesium-sulfate-in-dextrose1-figure-2-jIM-1581.jpg

Magnesium Sulfate In Dextrose

Recalling Firm: Hospira Inc.

Recall Initiation Date: Friday March 6th, 2015

Reason for Recall: Labeling: Wrong Bar Code: There is a potential for some units to be mislabeled with an incorrect barcode on the immediate container that scans as heparin sodium 2000 USP units/1000 mL in 0.9% in sodium chloride injection.


http://dailymed.nlm.nih.gov/dailymed/image.cfm?setid=91bc1221-4191-4970-88e3-a1659bc75392&name=carboinj91063-figure-02.jpg

Carboplatin

Recalling Firm: Mylan Institutional LLC

Recall Initiation Date: Wednesday March 18th, 2015

Reason for Recall: Presence of Particulate Matter: visible foreign particulate matter observed during testing of retention samples.


http://dailymed.nlm.nih.gov/dailymed/image.cfm?setid=b9be45c5-49db-4ec0-ae4f-aac0fe835829&name=image-02.jpg

Lidocaine Hydrochloride

Recalling Firm: Hospira Inc.

Recall Initiation Date: Friday April 18th, 2014

Reason for Recall: Presence of Particulate Matter: Confirmed customer complaint that orange and black particulates, identified as iron oxide, were found embedded within the glass vial and floating in solution.


http://dailymed.nlm.nih.gov/dailymed/image.cfm?setid=6ce99730-887e-410e-8ac9-f9c96d0f4814&name=A1240-18.jpg

Mucus Relief

Recalling Firm: Hospira Inc.

Recall Initiation Date: Friday April 18th, 2014

Reason for Recall: Presence of Particulate Matter: Confirmed customer complaint that orange and black particulates, identified as iron oxide, were found embedded within the glass vial and floating in solution.


http://dailymed.nlm.nih.gov/dailymed/image.cfm?setid=f2b9ed4a-5025-400c-8335-d717758ac84f&name=A3207-22.jpg

A3207-22 Portex Amniocentesis 22g Quincke

Recalling Firm: Hospira Inc.

Recall Initiation Date: Friday April 18th, 2014

Reason for Recall: Presence of Particulate Matter: Confirmed customer complaint that orange and black particulates, identified as iron oxide, were found embedded within the glass vial and floating in solution.


http://dailymed.nlm.nih.gov/dailymed/image.cfm?setid=829e3bd1-fb1c-4613-9db3-9a89ef8e2c0c&name=mlk02-0000-05.jpg

Mlk F4 Kit

Recalling Firm: Hospira Inc.

Recall Initiation Date: Friday April 18th, 2014

Reason for Recall: Presence of Particulate Matter: Confirmed customer complaint that orange and black particulates, identified as iron oxide, were found embedded within the glass vial and floating in solution.


http://dailymed.nlm.nih.gov/dailymed/image.cfm?setid=1fe460e7-208d-410e-84c5-cd63005cff47&name=mar09-0000-04.jpg

Marlido 25 Kit

Recalling Firm: Hospira Inc.

Recall Initiation Date: Friday April 18th, 2014

Reason for Recall: Presence of Particulate Matter: Confirmed customer complaint that orange and black particulates, identified as iron oxide, were found embedded within the glass vial and floating in solution.


http://dailymed.nlm.nih.gov/dailymed/image.cfm?setid=3b2dd84e-cee8-4e58-d494-395a65a353a0&name=lidocaine-hydrochloride-injection-usp1-figure-10-jRL-1045.jpg

Lidocaine Hydrochloride

Recalling Firm: Hospira Inc.

Recall Initiation Date: Friday April 18th, 2014

Reason for Recall: Presence of Particulate Matter: Confirmed customer complaint that orange and black particulates, identified as iron oxide, were found embedded within the glass vial and floating in solution.


http://dailymed.nlm.nih.gov/dailymed/image.cfm?setid=ffbc9885-eae2-4450-9c24-e7a20a30e1a7&name=MM2.jpg

Lidocaine Hydrochloride

Recalling Firm: Hospira Inc.

Recall Initiation Date: Friday April 18th, 2014

Reason for Recall: Presence of Particulate Matter: Confirmed customer complaint that orange and black particulates, identified as iron oxide, were found embedded within the glass vial and floating in solution.


http://dailymed.nlm.nih.gov/dailymed/image.cfm?setid=22ebe9b5-91d9-43eb-a52c-1523def30159&name=61699-4276-2_LABEL.jpg

Lidocaine Hydrochloride

Recalling Firm: Hospira Inc.

Recall Initiation Date: Friday April 18th, 2014

Reason for Recall: Presence of Particulate Matter: Confirmed customer complaint that orange and black particulates, identified as iron oxide, were found embedded within the glass vial and floating in solution.


http://dailymed.nlm.nih.gov/dailymed/image.cfm?setid=afd7c91b-3283-49e7-b79f-1c8d0c1a53bd&name=afd7c91b-3283-49e7-b79f-1c8d0c1a53bd-02.jpg

Lidocaine Hydrochloride

Recalling Firm: Hospira Inc.

Recall Initiation Date: Friday April 18th, 2014

Reason for Recall: Presence of Particulate Matter: Confirmed customer complaint that orange and black particulates, identified as iron oxide, were found embedded within the glass vial and floating in solution.


http://dailymed.nlm.nih.gov/dailymed/image.cfm?setid=84da743b-1ed2-4ddd-acd3-86fafd3d65c7&name=Label1.jpg

Lidocaine Hydrochloride

Recalling Firm: Hospira Inc.

Recall Initiation Date: Friday April 18th, 2014

Reason for Recall: Presence of Particulate Matter: Confirmed customer complaint that orange and black particulates, identified as iron oxide, were found embedded within the glass vial and floating in solution.


http://dailymed.nlm.nih.gov/dailymed/image.cfm?setid=632a8105-9cb2-44ba-8c10-2a1efd6ac960&name=gemcitabineforinj-figure-02.jpg

Gemcitabine Hydrochloride

Recalling Firm: Mylan Institutional LLC

Recall Initiation Date: Monday March 23rd, 2015

Reason for Recall: Presence of Particulate Matter: visible foreign particulate matter observed during testing of retention samples.


http://dailymed.nlm.nih.gov/dailymed/image.cfm?setid=f55bd888-5e01-474d-871b-24654c070178&name=image-01.jpg

Amiodarone Hydrochloride

Recalling Firm: Baxter Healthcare Corp.

Recall Initiation Date: Friday July 17th, 2015

Reason for Recall: Presence of Particulate Matter: Customer complaint for an insect found free floating inside a single bag for each lot recalled.


http://dailymed.nlm.nih.gov/dailymed/image.cfm?setid=553ab968-382f-4396-bd1e-85a8845ac421&name=MM1.jpg

Sodium Chloride

Recalling Firm: Baxter Healthcare Corp.

Recall Initiation Date: Friday July 17th, 2015

Reason for Recall: Presence of Particulate Matter: Customer complaint for an insect found free floating inside a single bag for each lot recalled.


http://dailymed.nlm.nih.gov/dailymed/image.cfm?setid=b90e0da7-f702-4f09-9488-74f2bb20e9ac&name=dd0007df-b7e7-4410-84a7-8bd5e5fffef5-02.jpg

Adrucil

Recalling Firm: Teva Pharmaceuticals USA

Recall Initiation Date: Friday July 24th, 2015

Reason for Recall: Presence of Particulate Matter: silcone rubber and fluorouracil crystals found floating in solution


http://dailymed.nlm.nih.gov/dailymed/image.cfm?setid=43b6accd-2d82-4b17-2d80-cce1018e6719&name=0pnt9prct-sodium-chloride-injection-usp4-figure-1-jIM-1693.jpg

Sodium Chloride

Recalling Firm: Hospira Inc.

Recall Initiation Date: Thursday March 5th, 2015

Reason for Recall: Presence of Particulate Matter: Confirmed finding of human hair floating in IV solution.


http://dailymed.nlm.nih.gov/dailymed/image.cfm?setid=19228ba2-098d-47d0-9029-804b4627f98d&name=mucinex-01.jpg

Mucinex Fast-max Day Time Severe Cold And Mucinex Fast-max Night Time Cold And Flu Maximum Strength

Recalling Firm: Reckitt Benckiser LLC

Recall Initiation Date: Wednesday April 15th, 2015

Reason for Recall: Labeling: Label Mix-Up; Bottles of Mucinex Fast-Max liquid are correctly labeled on the front of the label, however the back of the bottle where the Drug Facts labeling is, is missing certain Active Ingredients such as acetaminophen, phenylephrine, dextromethorphan, diphenhydramine, and/or guaifenesin. As a result certain safety warnings associated with those ingredients may also be missing.


http://dailymed.nlm.nih.gov/dailymed/image.cfm?setid=c902b4fc-c71c-4ef2-b5cb-6c2bd019acbc&name=mucinex-01.jpg

Mucinex Fast-max Cold

Recalling Firm: Reckitt Benckiser LLC

Recall Initiation Date: Wednesday April 15th, 2015

Reason for Recall: Labeling: Label Mix-Up; Bottles of Mucinex Fast-Max liquid are correctly labeled on the front of the label, however the back of the bottle where the Drug Facts labeling is, is missing certain Active Ingredients such as acetaminophen, phenylephrine, dextromethorphan, diphenhydramine, and/or guaifenesin. As a result certain safety warnings associated with those ingredients may also be missing.


http://dailymed.nlm.nih.gov/dailymed/image.cfm?setid=c8758d46-17c8-4fcd-9a0f-e73a2dad6860&name=image-01.jpg

Dextrose

Recalling Firm: Baxter Healthcare Corp.

Recall Initiation Date: Tuesday March 24th, 2015

Reason for Recall: Presence of Particulate Matter: Products recalled due to presence of particulate matter (metal)


http://dailymed.nlm.nih.gov/dailymed/image.cfm?setid=3bb406a9-f5cb-403a-b1bb-5c4facbea3d5&name=image-02.jpg

Protonix Delayed-release

Recalling Firm: Baxter Healthcare Corp.

Recall Initiation Date: Tuesday March 24th, 2015

Reason for Recall: Presence of Particulate Matter: Products recalled due to presence of particulate matter (metal)


http://dailymed.nlm.nih.gov/dailymed/image.cfm?setid=fbc01464-8885-4075-af41-911ffec5ae92&name=image-02.jpg

Sodium Chloride

Recalling Firm: Baxter Healthcare Corp.

Recall Initiation Date: Friday July 17th, 2015

Reason for Recall: Presence of Particulate Matter: Customer complaint for an insect found free floating inside a single bag for each lot recalled.


http://dailymed.nlm.nih.gov/dailymed/image.cfm?setid=fdf52dca-732c-4a1a-9475-e9e1e3af4ce8&name=gemcitabine-for-inj-mylan-figure-06.jpg

Gemcitabine Hydrochloride

Recalling Firm: Mylan Institutional LLC

Recall Initiation Date: Monday March 23rd, 2015

Reason for Recall: Presence of Particulate Matter: visible foreign particulate matter observed during testing of retention samples.


http://dailymed.nlm.nih.gov/dailymed/image.cfm?setid=eb269566-5024-4495-fb86-db0339bd0488&name=lactated-ringers-injection-usp1-figure-3-JIM-0036.jpg

Lactated Ringers And Dextrose

Recalling Firm: Hospira Inc.

Recall Initiation Date: Thursday July 10th, 2014

Reason for Recall: Non-Sterility: Confirmed customer complaint of particulate matter floating within the solution of the primary container, consistent with mold.