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

Recall Z-0162-2018 — Sensicare Green Surgical Glove, PI, LF, PF. Packaged in a poly/poly peel pouch with Sunoco films, sterile. Surgical glove.

U.S. FDA — Device Enforcement · United States · 2017-10-23 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0162-2018
Date of alert
2017-10-23
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Medline Industries Inc
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
701893369485
Reported risk: Possible open seal on top portion of the package. Could cause breach of sterility.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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