Orthopedic Pack, Model: 88041-12 AC2424601B 09/02/2029 Universal Pack, Model: 77165-06 AC2424902B 09/05/2029
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
Surgical drape packs may have open seals, which may compromise the sterility of the product.
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
Worldwide - US Nationwide distribution in the states of GA, AL, PA and the countries of MX.
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