Covidien recalls McGrath Mac 2 disposable laryngoscope blades (REF 350-084-000) due to potential condensation causing blurred vision during use. Affected items have specific UDI and lot numbers.
Laryngoscope blades may contain an ineffective application of anti-fog agent which may result in condensation accumulating causing the screen to be blurred or obscured.
Covidien is recalling McGrath Mac 2 disposable laryngoscope blades that may have condensation issues, blurring the view during medical procedures. This could affect patient safety if the blade isn't clearly visible during surgery.
The blades may have an ineffective anti-fog coating that leads to condensation buildup. This can blur the view during critical medical procedures like intubation, potentially affecting the surgeon's ability to see the airway.
Healthcare professionals using the McGrath Mac 2 laryngoscope blades for medical procedures are most at risk. Patients undergoing surgery may be affected if the blade becomes obscured.
Check for the product name 'McGrath Mac 2', reference number 350-084-000, and sterile packaging. Affected items have UDI 10884521824386 and lot number 22102001.
Look for the reference number 350-084-000 and UDI 10884521824386 on the blade packaging.
The blades may have an ineffective anti-fog coating that causes condensation, potentially blurring the view during medical procedures.
Check for the reference number 350-084-000 and UDI 10884521824386 on the blade packaging.
The recall record does not specify a remedy, so contact your healthcare provider for guidance.
We’ve drafted a message you can send Covidien to request your refund or repair — edit it as you like.
Subject: Recall Z-0169-2024 — Covidien Covidien Hello, I own a Covidien that is covered by recall Z-0169-2024 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
