FDA-Device2026-10-07Class IIPROCESSING DEFECT
Performance Pro blue nitrile examination gloves recalled for tears, missing fingers, and contamination risk
What this means
Performance Pro blue nitrile patient examination gloves may have defects including tears, missing fingers, or debris inside the gloves. Defective gloves can expose healthcare workers and patients to infectious pathogens or chemical agents.
- Check glove boxes for lot numbers matching the FDA recall list (AO01306, AO01307, AO01313, and others listed on FDA.gov)
- Stop using any gloves from affected lots
- Contact your supplier or American Nitrile Operations for replacement gloves
- Report any injuries or exposures to the FDA MedWatch program
The agency's original wording
Hazard
Gloves may exhibit defects such as tears, missing fingers, and debris. Use of defective gloves may lead to healthcare personnel and patient exposure to infectious pathogens leading to infection or cross-contamination, or exposure to chemical agents leading to irritation or systemic toxicities.
Intended for
All ages
Illnesses reported
None reported
Sold states
US Nationwide distribution.
Affected count
99,724,000
Manufactured in
3500 Southwest Blvd, Grove City, OH, United States
Products
Brand Name: Performance Pro Product Name: Performance Pro Model/Catalog Number: 72-RM50601,72-RM50602, 72-RM50603,72-RM50604 Product Description: Blue Nitrile Patient examination gloves
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-3289-2026More American Nitrile Operations recalls
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