O&M HALYARD, INC.: Medical Device Recall in 2025 - (Recall #: Z-0983-2025)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2025.

Data Source: FDA.

Product Description:

Brand Name: HALYARD Product Name: Laparotomy Pack Model/Catalog Number: 88231 Software Version: N/A Product Description: Laparotomy Pack Component: N/A

Product Classification:

Class II

Date Initiated: November 26, 2024

Date Posted: January 29, 2025

Recall Number: Z-0983-2025

Event ID: 95920

Reason for Recall:

Elevated residues of anti-block/slip additive used in manufacturing found within sterile packaging.

Status: Ongoing

Product Quantity: 1440 units

Code Information:

Model No 88231; UDI-DI: 30680651882319; Lot Number: AC2335502D; Exp Date 21-12-28

Distribution Pattern:

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.

Voluntary or Mandated:

Voluntary: Firm initiated