Recall Z-0729-2025

O&M Halyard, Inc. · initiated November 8, 2024

Class II Open, Classified

Class II – products that might cause a temporary health problem or pose a slight threat of a serious nature

Product

O&M Halyard SOFT TOUCH II Surgical Mask, Blue-Disposable surgical mask Product Code: 47500

Codes / lots: UDI-DI: 20680651475002 Lot Number: AM4119961 Exp. Date: 2029-04-28

Reason for recall

Not meeting the bioburden testing requirements of EN 14683 required for masks sold in Europe. Face masks sold in the United States are not required to meet this standard. However, if the standard is printed on the packaging, compliance is required.

FDA-determined cause: Nonconforming Material/Component

Action taken

O&M Halyard issued Urgent: Product Field Action via email on 11/8/24 to Distributors and End-Users. Letter states reason for recall, health risk and action to take: Customers (end-users): 1. REVIEW your inventory for the affected product code and specific lot number. 2. DESTROY or DISCARD the product per the facility s standard disposal procedure for face masks. 3. COMMUNICATE this Field Action to staff to ensure awareness of it. 4. RETURN the completed Field Action Response Form to OMRA_RECALLS@owens-minor.com as soon as possible even if you have no current product inventory. 5. Any adverse events associated with the use of the affected product should be reported to complaints@owens-minor.com. 6. If you received product from a distributor, please contact the distributor or your sales representative with any questions you may have. Distributors: 1. REVIEW your inventory for the affected product code and specific lot number. 2. DESTROY or DISCARD the product per the facility s standard disposal procedure for face masks. 3. COMMUNICATE this voluntary Field Action to staff to ensure awareness of it. 4. 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. 5. Any adverse events associated with the use of the affected product should be reported to complaints@owens-minor.com. 6. RETURN the completed Field Action Response Form to OMRA_RECALLS@owens-minor.com as soon as possible even if you have no current product inventory. If you have any questions, please email OMRA_RECALLS@owens-minor.com using the Event # FA-2024-034 in the header of the response.

Details

Recall number
Z-0729-2025
Initiated
November 8, 2024
Posted by FDA
December 20, 2024
Product code
FXX – Mask, Surgical
Quantity
637 cases
Distribution
Nationwide
Recalling firm
O&M Halyard, Inc., Mechanicsville, VA

Official FDA recall record

Other products in the same recall event

RecallProductInitiated
Z-0728-2025 Class IIO&M Halyard Procedure Mask with SO SOFT* Earloops, Yellow-Disposable surgical mask…Not meeting the bioburden testing requirements of EN 14683 required for masks sold in Europe. Face masks… 11/08/2024Open, Classified