Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Brand Name: HALYARD Product Name: Laparotomy Pack Model/Catalog Number: 88231 Recalled by O&M HALYARD, INC. Due to Elevated residues of anti-block/slip additive used in manufacturing...
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 O&M HALYARD, INC. directly.
Affected Products
Brand Name: HALYARD Product Name: Laparotomy Pack Model/Catalog Number: 88231 Software Version: N/A Product Description: Laparotomy Pack Component: N/A
Quantity: 1440 units
Why Was This Recalled?
Elevated residues of anti-block/slip additive used in manufacturing found within sterile packaging.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About O&M HALYARD, INC.
O&M HALYARD, INC. has 5 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report