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

Recall Z-2368-2015 — HUDSON RCI, Sheridan Sher-I-BRONCH, Endobronchial Tube (Right sided), Sizes: 28 Fr., 35 Fr., 37 Fr., 39 Fr. and 41 Fr., Rx Only, Sterile. Intended for use in thoracic surgery, bronchospirometry, for the administration of bronchial anesthesia and other uses commonly requiring bronchial intubation.

U.S. FDA — Device Enforcement · United States · 2015-06-01 · Class I

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2368-2015
Date of alert
2015-06-01
Country / jurisdiction
United States
Risk level
Class I
Risk type
recall
Brand
Teleflex Medical
Product category
device
Product type
Devices
Reported risk: The double swivel connector may crack or separate on the endobronchial tube.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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