FDAClass II · Medical device · Recall Z-2230-2026 · Recalled June 3, 2026

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

Agency report date: June 3, 2026.

1. Compare your item

This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.

Product named: Halyard Purezero Ultraviolet Nitrile Exam Gloves Reference Numbers
Company / brand: O&M HALYARD
Lot / serial / date codes: 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)
Distribution: US Nationwide distribution in the states of GA, CA, NJ, MA, NY, NC.

Agency product description and boundaries

Halyard Purezero Ultraviolet Nitrile Exam Gloves Reference Numbers: 48771 (XS), 48772 (Sm.), 48773 (Md.), 48774 (Lg.), 48775 (Xl)

Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.

If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.

2. Agency hazard and consumer action

FDA reports: Nitrile Exam Glove failed to meet specifications chemical permeation performance.

No consumer remedy instructions are supplied in this record. Check the official notice and listed company contact for the agency’s current instructions.

Class II: may cause temporary or medically reversible health consequences.

Affected product: Halyard Purezero Ultraviolet Nitrile Exam Gloves Reference Numbers recall status

3. Open the official notice or contact

View the official FDA enforcement record (openFDA) ↗

Official recall ID: Z-2230-2026
Brand: All O&M HALYARD recalls
Classification: Class II
Units affected: 452,500 units
Recall status: Ongoing
Initiated: Voluntary: Firm initiated

Affected products

Halyard Purezero Ultraviolet Nitrile Exam Gloves Reference Numbers recall status

Companies & origin

Recalling firm location: Alpharetta, GA, United States
Firm address: 1220 Old Alpharetta Rd Ste 320, 30005-3946

Identifying details (verbatim from the notice)

Product codes / lots: 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)
Distribution: US Nationwide distribution in the states of GA, CA, NJ, MA, NY, NC.
Firm notified the public via: Letter
FDA event ID: 98805
Recall initiated: April 13, 2026
FDA classified: May 22, 2026
FDA report date: June 3, 2026

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Verify with the official sources:

CPSC — consumer products ↗ (aggregated here)
NHTSA — vehicles, car seats, tires ↗ (aggregated here; use NHTSA's VIN lookup to check a specific vehicle)
FDA — food, drugs, medical devices ↗ (aggregated here)
USDA FSIS — meat, poultry & processed egg products ↗ (not aggregated here)
Recalls.gov — the U.S. government’s all-agency portal ↗

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Source: U.S. Food & Drug Administration. Agency excerpts come from the public data feed and may omit tables or later changes; the linked government source is authoritative. Source last checked October 22, 2026 at 6:00 PM UTC. Record retrieved September 1, 2026 at 6:00 PM UTC.

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