O&M HALYARD INC recalls Orthopedic Pack

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

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

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 complaints@owens-minor.com. 5) RETURN the completed Field Action Response Form to GM-OMRA_RECALLS@owens-minor.com 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 GM-OMRA_RECALLS@owens-minor.com. If you have any questions, please email GM-OMRA_RECALLS@owens-minor.com using the Event # FA-2025-015 in the header of the response

• FDA enforcement recordOfficial FDA database entry for Z-2520-2025
• FDA 510(k) clearance · K083234The device's official FDA premarket clearance record
• FDA device classification · KKXOfficial FDA classification for this device type
• CFR regulation · 21 CFR 878.4370The federal regulation governing this device
• FDA recall announcementSearch FDA.gov for the official press announcement
• Find O&M HALYARD INCSearch for the manufacturer's official notice
• News coverageRecent reporting on this recall and manufacturer
• openFDA data recordThe raw JSON record this page is built from

Source: U.S. FDA openFDA device enforcement reports. This summary is informational and may lag or differ from the official record. Always verify against the FDA before acting.