TELEFLEX LLC 2023-07-05 Health critical FDA
Health · FDA · Recall #FDA-Z-1959-2023
Endotracheal Tube oral/nasal Magill, High Volume, Low Pressure Cuff, REF 112080060 Recall
Issued July 5, 2023 · TELEFLEX LLC
In July 2023, TELEFLEX LLC recalled the Endotracheal Tube oral/nasal Magill, High Volume, Low Pressure Cuff, REF 112080060, 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
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
What you should do
- 1 Stop using Endotracheal Tube oral/nasal Magill, High Volume, Low Pressure Cuff, REF 112080060 right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact TELEFLEX LLC 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
- TELEFLEX LLC
- Category
- Health
- Recall date
- July 5, 2023
- Units affected
- Not reported
- Sold at
- US Nationwide distribution including Puerto Rico.
- Recall number
- FDA-Z-1959-2023
- Made in
- United States
- Issuing agency
- FDA
In context
- TELEFLEX LLC has 12 recalls in our database, including 11 rated Critical.
- We're tracking 3,576 Health recalls in our database.
- This is the 903rd Health recall we've logged in 2023.