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

Recall Z-0366-2017 — Professional Hospital Supply, Inc Custom Packaging containing the Devon Light Glove Item Number Description 380789003 SURE SET SINGLE BASIN PACK 400383006 MAJOR BASIN PACK 400383007

U.S. FDA — Device Enforcement · United States · 2016-09-29 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0366-2017
Date of alert
2016-09-29
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Covidien LLC
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
380789003
Reported risk: Added Instructions for Use: After application, inspect the Light Glove for barrier integrity
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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