Reported Jan 18, 2023 · Ongoing
COVIDIEN Emprint Ablation Catheter with Thermosphere Technology, Bronchoscopic Ablation, REF CA108L1
Covidien, LLC
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Covidien, LLC · 161 Cheshire Ln N Ste 100 · Minneapolis, MN · 55441-5433
Is this the product you have?
- COVIDIEN Emprint Ablation Catheter with Thermosphere Technology, Bronchoscopic Ablation, REF CA108L1
- Lot codes and dates
- UDI/DI (GTIN)10884521825765
- Lot Number520200
- Amount recalled
- 21 units
Why it was recalled
The product is labeled with the incorrect expiration date.
This product could cause temporary or reversible health problems — stop using it.
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