Reported Jan 29, 2025 · Ongoing
Brand Name: HALYARD Product Name: Laparotomy Pack Model/Catalog Number: 88231 Software Version: N/A Product…
O&m Halyard, Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: O&M HALYARD, INC. · 9120 Lockwood Blvd · Mechanicsville, VA · 23116-2015
Is this the product you have?
- Brand NameHALYARD
- Product NameLaparotomy
- Pack Model/Catalog Number88231
- Software VersionN/A
- Product DescriptionLaparotomy
- Pack ComponentN/A
- Lot codes and dates
- Model No 88231
- UDI-DI30680651882319
- Lot Number
AC2335502DExp Date 21-12-28
- Amount recalled
- 1440 units
Where it was sold
Why it was recalled
Elevated residues of anti-block/slip additive used in manufacturing found within sterile packaging.
This product could cause temporary or reversible health problems — stop using it.
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