FDA records indicate that there are no current recalls for this drug.
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Bionect Foam Recall
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Questions & Answers
Side Effects & Adverse Reactions
If conditions worsens, consult your physician immediately. Keep this product out of the reach of children. The prolonged use of the product may give rise to sensitization phenomena. Should this happen, discontinue the treatment and follow a suitable therapy. Do not use the product after expiration date reported on the package.
WarningBionect Foam - contents under preassure, do not puncture or incinerate. Do not store at temperatures above 120F. Protect from freezing. Keep out of reach of children
Legal Issues
There is currently no legal information available for this drug.
FDA Safety Alerts
There are currently no FDA safety alerts available for this drug.
Manufacturer Warnings
There is currently no manufacturer warning information available for this drug.
FDA Labeling Changes
There are currently no FDA labeling changes available for this drug.
Uses
Bionect is indicated for the dressing and management of partial to full thickness dermal ulcers (pressure sores, venous stasis ulcers, arterial ulcers, diabetic ulcers), wounds including cuts, abrasions, donor sites, and post-operative incisions, irritations of the skin, and first and second degree burns, The dressing is intended to cover a wound or burn on a patient's skin, and protect against abrasion, friction and desiccation.
History
There is currently no drug history available for this drug.
Other Information
Bionect Foam is a soft white foam, which, at rest, takes the form of a clear, pale yellow liquid. The principal component is the sodium salt of hyaluronic acid (0.2%). The sodium hyaluronate (Hyalastine) is derived from a natural fermentation process. Hyaluronic acid is a biological polysaccharide (glycosaminoglycan) and is a major component of the extracellular matric of the connective tissues.
Sources
Bionect Foam Manufacturers
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Innocutis Holdings Llc
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