American Nitrile Operations LLC recalls Brand Name: Opportunity Pro Product Name: Opportunity Pro Model/Catalog Number: 72-50800

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 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.

• FDA enforcement recordOfficial FDA database entry for Z-3291-2026
• FDA 510(k) clearance · K220825The device's official FDA premarket clearance record
• FDA device classification · LZAOfficial FDA classification for this device type
• CFR regulation · 21 CFR 880.6250The federal regulation governing this device
• FDA recall announcementSearch FDA.gov for the official press announcement
• Find American Nitrile Operations LlcSearch for the manufacturer's official notice
• News coverageRecent reporting on this recall and manufacturer
• openFDA data recordThe raw JSON record this page is built from

Source: U.S. FDA openFDA device enforcement reports. This summary is informational and may lag or differ from the official record. Always verify against the FDA before acting.