Fresh Recalls

O&M HALYARD recalls

Recall found. O&M HALYARD is named in FDA Class II recall Z-2230-2026 covering Halyard Purezero Ultraviolet Nitrile Exam Gloves Reference Numbers. Hazard: Nitrile Exam Glove failed to meet specifications chemical permeation performance. Identifying details: REF: 48771/UDI: 30680651487712 (Package)20680651487715 (Primary)90680651487714 (Unit of Use) ; 48772/30680651487729 (Package)20680651487722 (Primary)90680651487721 (Unit of Use);48773/30680651487736 (Package)20680651487739 (Primary)90680651487738 (Unit of Use);48774/UDI: 30680651487743 (Package)20680651487746 (Primary) 90680651487745 (Unit of Use);48775/UDI:30680651487750 (Package)20680651487753 (Primary)90680651487752 (Unit of Use). Status: Ongoing.

Models with recalls

Halyard Purezero Ultraviolet Nitrile Exam Gloves Reference Numbers (1)

All O&M HALYARD recalls

FDA Class II · Medical device · June 3, 2026

Halyard Purezero Ultraviolet Nitrile Exam Gloves Reference Numbers recall — O&M HALYARD INC

Nitrile Exam Glove failed to meet specifications chemical permeation performance.

Official ID Z-2230-2026 · Official record ↗

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Compiled from official public-domain government data. Last checked October 22, 2026 at 6:00 PM UTC.