FDA recall Z-2230-2026

O&M HALYARD INC · Class II · device

Product

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

Reason for recall

Nitrile Exam Glove failed to meet specifications chemical permeation performance.

Distribution

US Nationwide distribution in the states of GA, CA, NJ, MA, NY, NC.

Key facts

Status
Ongoing
Initiation date
2026-04-13
Report date
2026-06-03
Voluntary/Mandated
Voluntary: Firm initiated
Location
Alpharetta, GA, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2230-2026