Baxter Healthcare Corp recalls COSEAL Surgical Sealant Kit, 8 mL, Product Code: 934072; For use in vascular reconstructions to achieve adjunctive hemo…
- Recall date
- May 12, 2016
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-1840-2016
- FDA classification
- Class II
- Brand / firm
- Baxter Healthcare Corp
- Sold / distributed
- Distributed US (nationwide) including Puerto Rico and in the Bahamas, Canada, and Singapore.
Why it was recalled
Potential for incomplete dissolution of the polyethylene glycol (PEG) component during the reconstitution of the product, which may affect the consistency of the hydrogel formation during use.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
COSEAL Surgical Sealant Kit, 8 mL, Product Code: 934072; For use in vascular reconstructions to achieve adjunctive hemostasis by mechanically sealing areas of leakage.
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