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

Recall Z-1179-2021 — VentStar Watertrap (N) 180-Drager Breathing Circuits/Anesthesia Sets Order Number: MP00363 - Product Usage: Breathing circuit for conduction of respiratory gases between anesthesia machine or ventilator and patient. Intended for single use only.

U.S. FDA — Device Enforcement · United States · 2021-01-29 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-1179-2021
Date of alert: 2021-01-29
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Draeger Medical, Inc.
Product category: device
Product type: Devices

Reported risk: Y-piece may become detached from the ventilation hose either before or during the ventilation process, a leak will be caused that can hinder ventilation of the patient.

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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Recall Z-1179-2021 — VentStar Watertrap (N) 180-Drager Breathing Circuits/Anesthesia Sets Order Number: MP00363 - Product Usage: Breathing circuit for conduction of respiratory gases between anesthesia machine or ventilator and patient. Intended for single use only.

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