Recall Z-1521-2022— Medtronic Xomed, Inc.

Name: FDA recall Z-1521-2022
Creator: U.S. Food and Drug Administration
Published: 2022-04-29

Class I · Ongoing

Class I FDA medical device recall by Medtronic Xomed, Inc., initiated 2022-04-29. FDA's recall record names no specific 510(k) clearance for this event. Product: NIM EMG Endotracheal Tube, Part Numbers: a) REF 8229307J b) REF 8229308J c) REF 8229306J. Reason: The firm received reports of events related to airway obstruction while using NIM Standard Reinforced EMG Endotracheal Tubes & NIM CONTACT Reinforced EMG Endotracheal Tubes..

Recalling firm: Medtronic Xomed, Inc.
Classification: Class I
Status: Ongoing
Initiated: 2022-04-29
Firm location: Jacksonville, FL, United States

Product description

NIM EMG Endotracheal Tube, Part Numbers: a) REF 8229307J b) REF 8229308J c) REF 8229306J

Reason for recall

The firm received reports of events related to airway obstruction while using NIM Standard Reinforced EMG Endotracheal Tubes & NIM CONTACT Reinforced EMG Endotracheal Tubes.

Data sourced from openFDA. This site is unofficial and independent of the FDA.