FDA recall record

O&M HALYARD Orthopedic Pack, Model: 88041-12 AC2424601B 09/02/2029 Universal Pack, Model recall — FDA Z-2520-2025

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

Class IIclassification
Z-2520-2025official record ID
Sep 10, 2025report date

Recall record at a glance

Official recordZ-2520-2025
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmO&M HALYARD Inc.
Report dateSep 10, 2025
Recall initiation dateJul 17, 2025
Quantity1316
LocationAlpharetta, GA, United States

Official product description

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

Why the product was recalled

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

Distribution information

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

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

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