Brand Name: Opportunity Pro Product Name: Opportunity Pro Model/Catalog Number: 72-50800, 72-50801,72-50802,72-50803,72-50804 Product Description: Blue Nitrile patient examination glove
FDA Recall Z-3291-2026 · Posted 2026-09-25
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Recalling FirmAmerican Nitrile Operations Llc
Recall StatusOpen, Classified
Product CodeLZA
Date Initiated2026-08-14
Product Quantity17,481,000
Reason for Recall
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.
Firm Action
Firm began notifying its VA customers on August 15, 2026 via email.
Instruction to Customers:
1. Immediately cease all use of the affected products.
2. Notify all users throughout your facility of the product recall.
3. Examine your inventory and immediately quarantine the affected lots to avoid accidental use
4 Contact distributor for replacement.
Root Cause
Process control
Distribution Pattern
US Nationwide distribution.
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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