PlainRecalls
FDA Devices Moderate Class II Ongoing

O&M Halyard Procedure Mask with SO SOFT* Earloops, Yellow-Disposable surgical mask Product Code: 47117

Reported: January 1, 2025 Initiated: November 8, 2024 #Z-0728-2025

Product Description

O&M Halyard Procedure Mask with SO SOFT* Earloops, Yellow-Disposable surgical mask Product Code: 47117

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.

Details

Recalling Firm
O&M HALYARD, INC.
Units Affected
211 cases
Distribution
Nationwide
Location
Mechanicsville, VA

Frequently Asked Questions

What product was recalled?
O&M Halyard Procedure Mask with SO SOFT* Earloops, Yellow-Disposable surgical mask Product Code: 47117. Recalled by O&M HALYARD, INC.. Units affected: 211 cases.
Why was this product recalled?
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.
Which agency issued this recall?
This recall was issued by the FDA Devices on January 1, 2025. Severity: Moderate. Recall number: Z-0728-2025.