Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
seprafilm¿ Procedure Pack ADHESION BARRIER Re-order Number: 5086-02 Product Usage: Recalled by Genzyme Corporation Due to Sterility of product may be compromised due to...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Genzyme Corporation directly.
Affected Products
seprafilm¿ Procedure Pack ADHESION BARRIER Re-order Number: 5086-02 Product Usage: Seprafilm Adhesion Barrier is indicated for use in patients undergoing abdominal or pelvic laparotomy as an adjunct intended to reduce the incidence, extent and severity of postoperative adhesions between the abdominal wall and the underlying viscera such as omentum, small bowel, bladder, and stomach, and between the uterus and surrounding structures such as tubes and ovaries, large bowel, and bladder.
Quantity: 3880units
Why Was This Recalled?
Sterility of product may be compromised due to packaging defect
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Genzyme Corporation
Genzyme Corporation has 6 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report