FDA Recall Open, Classified

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

Recall: Z-2520-2025 · Initiated July 17, 2025

Recall

Recall Number
Z-2520-2025
Event Number
97394
Firm
O & M HALYARD INC
FEI Number
3014421917
Product Code
KKX
Status
Open, Classified
Root Cause
Process control
Initiated
July 17, 2025
Posted
September 4, 2025
Address
1220 Old Alpharetta Rd, Ste 320, Alpharetta, GA, 30005-3946

Description

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

Reason

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

Action

On 7/17/2025, Field Action Customer Notifications were emailed to customers who were asked to do the following: 1) DESTROY or DISCARD the product available in your inventory per the facility's standard disposal procedure for surgical packs. 2) COMMUNICATE this Field Action to staff to ensure awareness of it. 3) If any of the affected lot identified above was further distributed, please ensure all end-users are appropriately notified of this Field Action and maintain records of effectiveness. 4) Any adverse events associated with the use of the affected product should be reported to [email protected]. 5) RETURN the completed Field Action Response Form to [email protected] as soon as possible even if you have no current product inventory. 6) If credit is requested, please get contact with the Customer Service team and send email to [email protected]. If you have any questions, please email [email protected] using the Event # FA-2025-015 in the header of the response

Distribution

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

Quantity

1316