Covidien recalls McGrath Mac 2 disposable laryngoscope blades with possible condensation causing blurred screens. 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. This could affect medical procedures requiring clear vision.
The blades may have an ineffective anti-fog coating, causing moisture to build up and blur the view. This could make it harder to see during medical procedures requiring clear vision.
Healthcare professionals using the blades for medical procedures. Patients undergoing procedures with these blades may be at risk if the view becomes blurred.
Check for the product name 'McGrath Mac 2', model REF: 350-017-000, and sterile EO, Rx Only. Look for UDI: 10884521816336 with lot numbers 22082207 or 22083101.
Verify the product name, model, and UDI/lot numbers to confirm if your blade is affected.
The blades may have an ineffective anti-fog coating, causing moisture to build up and blur the view during use.
Check the product details to see if your blade is affected; if so, contact the manufacturer for guidance.
The recall record does not mention a specific remedy or fix.
We’ve drafted a message you can send Covidien to request your refund or repair — edit it as you like.
Subject: Recall Z-0168-2024 — Covidien Covidien Hello, I own a Covidien that is covered by recall Z-0168-2024 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.
