Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
SURGICEL FIBRILLAR 1INX2IN(2.5CMX5.1CM) Recalled by Ethicon Sarl, a Johnson & Johnson Company Due to Some foil pouches were found torn open, impacting...
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 Ethicon Sarl, a Johnson & Johnson Company directly.
Affected Products
SURGICEL FIBRILLAR 1INX2IN(2.5CMX5.1CM), Product Number: 1961
Quantity: 450,793 units (65,950 US, 384,843 OUS)
Why Was This Recalled?
Some foil pouches were found torn open, impacting the sterile barrier which was traced to a specific machine used during product packaging.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Ethicon Sarl, a Johnson & Johnson Company
Ethicon Sarl, a Johnson & Johnson Company has 2 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report