Medtronic Xomed recalls specific NIM CONTACT EMG Endotracheal Tubes due to reports of airway obstruction. Affected units have part numbers REF 8229506-8229508 and UDI codes listed. Consumers should check their tubes for these identifiers.
The firm received reports of events related to airway obstruction while using NIM Standard Reinforced EMG Endotracheal Tubes & NIM CONTACT Reinforced EMG Endotracheal Tubes.
Medtronic Xomed is recalling NIM CONTACT EMG Endotracheal Tubes with part numbers REF 8229506, REF 8229507, and REF 8229508 due to reports of airway obstruction. This could lead to serious breathing difficulties if the tube becomes blocked during medical use.
The tubes can become blocked during medical use, leading to airway obstruction. This may cause breathing difficulties or other serious complications if the tube is not properly functioning.
Healthcare professionals using these tubes during medical procedures are most at risk. Patients receiving these tubes for breathing support may also be affected if the tube becomes obstructed.
Check for part numbers REF 8229506, REF 8229507, or REF 8229508 on the tube packaging or label. Also look for the unique device identifiers (UDIs) listed: 00643169789555, 00643169789562, 00643169789579, 00763000745844, 00763000745851, 00763000745868, 00763000882419, 00763000882426, 00763000882433.
Look for part numbers REF 8229506, REF 8229507, or REF 8229508 on the tube packaging or label.
Check for the listed unique device identifiers (UDIs) on the tube packaging or label.
Part numbers REF 8229506, REF 8229507, and REF 8229508 are affected.
Check for part numbers REF 8229506, REF 8229507, or REF 8229508 on the tube packaging or label, and look for the listed unique device identifiers (UDIs).
The tubes can become blocked during medical use, leading to airway obstruction and potential breathing difficulties.
We’ve drafted a message you can send Medtronic Xomed to request your refund or repair — edit it as you like.
Subject: Recall Z-1519-2022 — Medtronic Xomed Medtronic Xomed Hello, I own a Medtronic Xomed that is covered by recall Z-1519-2022 from Medtronic Xomed. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
