Halyard Purezero Ultraviolet Nitrile Exam Gloves Reference Numbers:… — Class II medical device recall Z-2230-2026
Ongoing recall by O&M HALYARD INC, reported 2026-06-03, distributed nationwide. Nitrile Exam Glove failed to meet specifications chemical permeation performance.
| Recall number | Z-2230-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | O&M HALYARD INC, Alpharetta, GA, United States |
| Recall initiated | 2026-04-13 |
| Classified | 2026-05-22 |
| Reported by FDA | 2026-06-03 |
| Distributed | Nationwide (US) |
| Quantity | 452,500 units |
| Reason classes | chemical contamination |
| UPC / GTIN / UDI-DI | 20680651487715, 20680651487722, 20680651487739, 20680651487746, 20680651487753, 30680651487712, 30680651487729, 30680651487736, 30680651487743, 30680651487750, 90680651487714, 90680651487721, 90680651487738, 90680651487745, 90680651487752 |
| Model numbers | 48771 |
Product
Halyard Purezero Ultraviolet Nitrile Exam Gloves Reference Numbers: 48771 (XS), 48772 (Sm.), 48773 (Md.), 48774 (Lg.), 48775 (Xl)
Reason for recall
Nitrile Exam Glove failed to meet specifications chemical permeation performance.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2230-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.