O&M HALYARD INC recalls Halyard Purezero Ultraviolet Nitrile Exam Gloves Reference Numbers: 48771
- Recalling company
- O&M HALYARD INC
- Product
- Halyard Purezero Ultraviolet Nitrile Exam Gloves Reference Numbers: 48771 (XS), 48772 (Sm.), 48773 (Md.), 48774 (Lg.), 48775 (Xl)
- Reason
- Nitrile Exam Glove failed to meet specifications chemical permeation performance.
- Classification
- Class II – may cause temporary or medically reversible health consequences
- Recall date
- Apr 13, 2026
- Reported
- Jun 3, 2026
- Distribution
- US Nationwide distribution in the states of GA, CA, NJ, MA, NY, NC.
- Status
- Ongoing
- Quantity
- 452,500 units
- Lot / 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)
- Company location
- Alpharetta, GA
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-2230-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-2230-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.