Class II — O&M HALYARD INC
| Recalling firm | O & M Halyard, Inc. |
|---|---|
| Registered facility | View this company's 11 registered facilities → (openFDA recall records do not name a specific facility) |
| Classification | Class II |
| Status | Ongoing |
| Reason | Nitrile Exam Glove failed to meet specifications chemical permeation performance. |
| Product | Halyard Purezero Ultraviolet Nitrile Exam Gloves Reference Numbers: 48771 (XS), 48772 (Sm.), 48773 (Md.), 48774 (Lg.), 48775 (Xl) |
| Quantity | 452,500 units |
| Distribution | US Nationwide distribution in the states of GA, CA, NJ, MA, NY, NC. |
| Initiated | 2026-04-13 |
| Classified | 2026-05-22 |
| Recall number | Z-2230-2026 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — O&M HALYARD INC (Z-2230-2026).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/98805/
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