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FDAFDA · Food and drugs·Recall number Z-2230-2026

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

Published June 3, 2026 · Recall initiated: April 13, 2026

Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.

What's the hazard

Nitrile Exam Glove failed to meet specifications chemical permeation performance.

What to do

Voluntary: Firm initiated · Letter

Recall details

Manufacturer
O&M HALYARD INC
Distributor
US Nationwide distribution in the states of GA, CA, NJ, MA, NY, NC.
Lot
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)
Risk classification
Class II
Area (FDA)
device
Country
United States

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