COVIDIEN Emprint Ablation Catheter with Thermosphere Technology, Bronchoscopic Ablation, REF CA108L1
Reported: January 18, 2023 Initiated: November 23, 2022 #Z-0955-2023
Product Description
COVIDIEN Emprint Ablation Catheter with Thermosphere Technology, Bronchoscopic Ablation, REF CA108L1
Reason for Recall
The product is labeled with the incorrect expiration date.
Details
- Recalling Firm
- Covidien, LLC
- Units Affected
- 21 units
- Distribution
- Foreign Distribution: Hong Kong
- Location
- Minneapolis, MN
Frequently Asked Questions
What product was recalled? ▼
COVIDIEN Emprint Ablation Catheter with Thermosphere Technology, Bronchoscopic Ablation, REF CA108L1. Recalled by Covidien, LLC. Units affected: 21 units.
Why was this product recalled? ▼
The product is labeled with the incorrect expiration date.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on January 18, 2023. Severity: Moderate. Recall number: Z-0955-2023.
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