Covidien 2024-08-28 Health critical FDA
Health · FDA · Recall #FDA-Z-2636-2024
McGrath Mac Video Laryngoscope, REF: 300-000-000 , Non-Sterile, Rx Only Recall
Issued August 28, 2024 · Covidien
In August 2024, Covidien recalled the McGrath Mac Video Laryngoscope, REF: 300-000-000 , Non-Sterile, Rx Only, a critical health recall reported by the FDA. Affected owners are eligible for a voluntary. Here is what the hazard is and exactly what to do about it.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Battery management system within Laryngoscope devices may deplete below the deign threshold which may result in thermal event followed by risk of explosion.
What you should do
- 1 Stop using McGrath Mac Video Laryngoscope, REF: 300-000-000 , Non-Sterile, Rx Only right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Covidien to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- Covidien
- Category
- Health
- Recall date
- August 28, 2024
- Units affected
- Not reported
- Sold at
- Worldwide - US Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA
- Recall number
- FDA-Z-2636-2024
- Made in
- United States
- Issuing agency
- FDA
In context
- Covidien has 2 recalls in our database, including 1 rated Critical.
- We're tracking 3,576 Health recalls in our database.
- This is the 737th Health recall we've logged in 2024.