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O&M HALYARD, INC. recalls Brand Name: HALYARD Product Name: Laparotomy Pack Model/Catalog Number: 88231 Software Version: N/A Product Descript
Recalled January 29, 2025 · FDA recall Z-0983-2025 · O&M HALYARD
Hazard
Elevated residues of anti-block/slip additive used in manufacturing found within sterile packaging. · FDA Class II
Units
1440 units
Sold at
US Nationwide distribution in the states of CO, FL, GA, HI, IA, IL, IN, KS, LA, MI, MN, MO, NC, NE, NY, TN, TX, VA, WI.
Description
Elevated residues of anti-block/slip additive used in manufacturing found within sterile packaging.
Product
Brand Name: HALYARD Product Name: Laparotomy Pack Model/Catalog Number: 88231 Software Version: N/A Product Description: Laparotomy Pack Component: N/A
Manufacturer(s)
O&M HALYARD, INC.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →