Avanos Medical, Inc. 2022-02-16 Health serious FDA
Health · FDA · Recall #FDA-Z-0566-2022
MIC* Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors - 20 Fr-PULL Recall
Issued February 16, 2022 · Avanos Medical, Inc.
In February 2022, Avanos Medical, Inc. recalled the MIC* Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors - 20 Fr-PULL, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
The External Retention Bolster contained in the kit may be a larger diameter than the tube.
What you should do
- 1 Stop using MIC* Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors - 20 Fr-PULL right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Avanos Medical, Inc. 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
- Avanos Medical, Inc.
- Category
- Health
- Recall date
- February 16, 2022
- Units affected
- Not reported
- Sold at
- Worldwide distribution - US Nationwide and the countries of Canada and Chile.
- Recall number
- FDA-Z-0566-2022
- Made in
- United States
- Issuing agency
- FDA
In context
- Avanos Medical, Inc. has 5 recalls in our database, including 1 rated Critical.
- We're tracking 3,576 Health recalls in our database.
- This is the 870th Health recall we've logged in 2022.