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

Recall Z-1211-2022 — Drager SafeStar 55, Catalog No. MP01790

U.S. FDA — Device Enforcement · United States · 2022-05-16 · Class I

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1211-2022
Date of alert
2022-05-16
Country / jurisdiction
United States
Risk level
Class I
Risk type
recall
Brand
Draeger Medical, Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
04048675026785
Reported risk: Possible occlusion of filters due to manufacturing error.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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