Covidien, LLC 2023-01-18 Health serious FDA
Health · FDA · Recall #FDA-Z-0955-2023
COVIDIEN Emprint Ablation Catheter with Thermosphere Technology, Bronchoscopic Ablation,… Recall
Issued January 18, 2023 · Covidien, LLC
In January 2023, Covidien, LLC recalled the COVIDIEN Emprint Ablation Catheter with Thermosphere Technology, Bronchoscopic Ablation,…, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
The product is labeled with the incorrect expiration date.
What you should do
- 1 Stop using COVIDIEN Emprint Ablation Catheter with Thermosphere Technology, Bronchoscopic Ablation,… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Covidien, 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
- Covidien, LLC
- Category
- Health
- Recall date
- January 18, 2023
- Units affected
- Not reported
- Sold at
- Foreign Distribution: Hong Kong
- Recall number
- FDA-Z-0955-2023
- Made in
- United States
- Issuing agency
- FDA
In context
- Covidien, LLC has 1 recall in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 903rd Health recall we've logged in 2023.