Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-2916-2020 — PROTEXIS Latex Micro Surgical Gloves Size 7.5 - Product Usage: This surgeon s glove is a disposable device made of natural rubber latex or synthetic rubber intended to be worn by operating room personnel to be a barrier protection from contamination. Various thickness for sensitivity or durability d

U.S. FDA — Device Enforcement · United States · 2020-07-29 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2916-2020
Date of alert
2020-07-29
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Cardinal Health 200, LLC
Product category
device
Product type
Devices
Reported risk: A degradation defect was found that could lead to holes and donning tears at the folding area around the cuffs.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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