Class II

Medical Device Recall: Orthopedic Pack, Model: 88041-12 AC2424601B 09/02/2029 Universal Pack, Model: 77165-06 AC2424902B 09/05/2029

O&M HALYARD INC · July 17, 2025

Reason for Recall

Surgical drape packs may have open seals, which may compromise the sterility of the product.

Distribution

Worldwide - US Nationwide distribution in the states of GA, AL, PA and the countries of MX.

States Affected

NATIONWIDE

Quantity Affected

1316

Source: FDA (openFDA Device Enforcement)

Recall number: Z-2520-2025

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.

O&M HALYARD INC Medical Device Recall: Orthopedic Pack, Model: 88041-12 AC2424601B 09/02/2029 Universal Pack, Model: 77165-06 AC2424902B 09/05/2029 | SafeCheck