O&M Halyard Procedure Mask with SO SOFT* Earloops, Yellow-Disposable surgical mask Product Code: 47117
Recall
- Recall Number
- Z-0728-2025
- Event Number
- 95804
- Firm
- O & M HALYARD, INC.
- FEI Number
- 3014527898
- Product Code
- FXX
- Status
- Open, Classified
- Root Cause
- Nonconforming Material/Component
- Initiated
- November 8, 2024
- Posted
- December 20, 2024
- Address
- 9120 Lockwood Blvd, Mechanicsville, VA, 23116-2015
Description
O&M Halyard Procedure Mask with SO SOFT* Earloops, Yellow-Disposable surgical mask Product Code: 47117
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.
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 [email protected] 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 [email protected]. 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 [email protected]. 6. RETURN the completed Field Action Response Form to [email protected] as soon as possible even if you have no current product inventory. If you have any questions, please email [email protected] using the Event # FA-2024-034 in the header of the response.
Nationwide
211 cases