Urgent Field Safety Notice For Eopa Arterial Cannula By Medtronic Inc
Recall Summary Medtronic Inc is recalling EOPA Arterial Cannula devices distributed in Germany and the EU due to an urgent safety issue. The cannula is a medical device used to access arteries. This is a Class I recall, which is the most serious classification.
- Recalling firm
- Medtronic Inc
- Product
- EOPA Arterial Cannula
- Reason
- Urgent Field Safety Notice for EOPA Arterial Cannula by Medtronic Inc
- Classification
- Class I
- Category
- medical device recall
- Country
- Germany
- Agency
- BFARM
- Recall date
- 2026-07-03
- Status
- Ongoing
- Distribution
- Germany / EU
Official recall notice from BFARM
Recall details on Nibble Recalls: https://trynibble.app/recalls/5c1d614c-3bb1-4ff8-bb1c-b0aee168bc0c