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All product recalls associated with O & M HALYARD INC.
Total Recalls
7
Past Year
1
Class I (Serious)
0
Most Recent
Jul 2025
Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.
Surgical drape packs may have open seals, which may compromise the sterility of the product.
Elevated residues of anti-block/slip additive used in manufacturing found within sterile packaging.
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.