FDAFDA · Food and drugs·Recall number Z-0955-2023
COVIDIEN Emprint Ablation Catheter with Thermosphere Technology, Bronchoscopic Ablation, REF CA108L1
Published January 18, 2023 · Recall initiated: November 23, 2022
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
The product is labeled with the incorrect expiration date.
What to do
Voluntary: Firm initiated · Visit
Recall details
- Manufacturer
- Covidien, LLC
- Distributor
- Foreign Distribution: Hong Kong
- Lot
- UDI/DI (GTIN): 10884521825765, Lot Number: 520200
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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