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

Recall Z-0044-2017 — Willy Rusch GmbH Tracheostomy Tube Set Cannulation of tracheotomised patients, particularly in the case of a narrow tracheostoma and narrow-lumen tracheas. When using cannulas with curr. For short term intermittent inflation.

U.S. FDA — Device Enforcement · United States · 2016-08-26 · Class I

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0044-2017
Date of alert
2016-08-26
Country / jurisdiction
United States
Risk level
Class I
Risk type
recall
Brand
Teleflex Medical
Product category
device
Product type
Devices
Reported risk: The connector may disconnect from the tracheostomy tube during use.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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