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Covidien, LLC recalls COVIDIEN Emprint Ablation Catheter with Thermosphere Technology, Bronchoscopic Ablation, REF CA108L1
Recalled January 18, 2023 · FDA recall Z-0955-2023 · Covidien
Hazard
The product is labeled with the incorrect expiration date. · FDA Class II
Units
21 units
Sold at
Foreign Distribution: Hong Kong
Description
The product is labeled with the incorrect expiration date.
Product
COVIDIEN Emprint Ablation Catheter with Thermosphere Technology, Bronchoscopic Ablation, REF CA108L1
Manufacturer(s)
Covidien, LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →