Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Surgipro Monofilament Polypropylene Sutures Product Description CP-535 SURGIPRO* 1 BLU Recalled by Covidien, LP Due to Sterile Barrier Breach of Breather Pouch may cause...
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 Covidien, LP directly.
Affected Products
Surgipro Monofilament Polypropylene Sutures Product Description CP-535 SURGIPRO* 1 BLU 100CM GS24 X36 CP-824 SURGIPRO* 1 BLU 150CM GS26 X24 CP-825 SURGIPRO* 2 BLU 150CM GS26 X24 VP-543 SURGIPRO* 2-0 BLU 120CM V20 DA
Quantity: 8604 units
Why Was This Recalled?
Sterile Barrier Breach of Breather Pouch may cause infection or vision loss for ophthalmic procedures in cases where there is direct patient contact
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Covidien, LP
Covidien, LP has 68 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report