Covidien recalls stolen McGRATH MAC Video Laryngoscopes (REF: 301-000-000) that failed quality tests. Defective units may cause failed laryngoscopy or intubation during medical procedures.
Defective video laryngoscopes that did not pass quality tests established for the product, that were designated for destruction, were stolen, and subsequently distributed for sale. Defective device use may result in failed laryngoscopy and/or intubation.
Covidien has recalled stolen McGRATH MAC Video Laryngoscopes that were designated for destruction but sold illegally. Using these defective devices may lead to failed laryngoscopy or intubation during medical procedures.
The recalled laryngoscopes failed quality tests and were stolen from Covidien. These defective devices may not function properly during medical procedures, potentially causing failed laryngoscopy or intubation, which could be life-threatening.
Healthcare professionals and medical facilities that own or use the recalled Stolen McGRATH MAC Video Laryngoscopes (REF: 301-000-000) are affected. Those with the listed serial numbers are at risk of failed intubation during critical medical procedures.
Check if your laryngoscope has a serial number listed in the provided range (e.g., 000063, 000076, 000085, etc.). The product was stolen and sold illegally, so it may lack proper packaging and labeling.
Immediately cease using the recalled Stolen McGRATH MAC Video Laryngoscopes (REF: 301-000-000) if you have a listed serial number.
Covidien recalled stolen McGRATH MAC Video Laryngoscopes that were designated for destruction but were sold illegally. These devices failed quality tests and may cause failed laryngoscopy or intubation.
Check if your laryngoscope's serial number is in the list of affected numbers provided in the recall notice (e.g., 000063, 000076, 000085, etc.).
Immediately stop using it and contact Covidien for further instructions.
We’ve drafted a message you can send Covidien to request your refund or repair — edit it as you like.
Subject: Recall Z-0144-2024 — Covidien Covidien Hello, I own a Covidien that is covered by recall Z-0144-2024 from Covidien. 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.
