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

Recall Z-0742-2019 — ID Circuit Watertrap (P) 180, Catalog Number MP01341 Breathing Circuits/Anesthesia Sets without a Water trap: Breathing circuit for conduction of respiratory gases between anesthesia machine or ventilator and patient. Intended for single use only. Breathing Circuits/Anesthesia Sets with Water t

U.S. FDA — Device Enforcement · United States · 2018-12-21 · Class I

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-0742-2019
Date of alert: 2018-12-21
Country / jurisdiction: United States
Risk level: Class I
Risk type: recall
Brand: Draeger Medical, Inc.
Product category: device
Product type: Devices

Reported risk: Incorrectly pre-assembled breathing circuit has potential for incorrect connection/short circuit of the breathing circuit

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

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

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