- Recalling firm
- O&M HALYARD INC
- Reason for recall
- Nitrile Exam Glove failed to meet specifications chemical permeation performance.
- Affected products (lot / model / serial)
- 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)
- Units affected
- 452,500 units
- Distribution pattern
- US Nationwide distribution in the states of GA, CA, NJ, MA, NY, NC.
- Firm location
- Alpharetta, GA, United States
- Recall type
- Voluntary: Firm initiated
- How the firm notified customers
- Letter
- Product type
- Devices
- Status
- Ongoing
- Recall number
- Z-2230-2026
- Recall initiated
- April 13, 2026
- FDA classification date
- May 22, 2026
- FDA report date
- June 3, 2026
- FDA event ID
- 98805
- Last updated on HTM Vibe
- July 24, 2026