Urgent Field Safety Notice For Endoflip System By Covidien Llc
Summary Covidien llc is issuing an urgent field safety notice for the EndoFLIP System, a medical device distributed in Germany and the EU. This is classified as a Class I recall, indicating a serious issue. The specific reason for the recall is not clearly detailed in the provided document information.
- Recalling firm
- Urgent Field Safety Notice for EndoFLIP System by Covidien llc , Download_VeroeffentlichtAm_EN 2026.05.19 PDF, 679KB, Fi
- Product
- s Tasks of the BfArM Risk assessment Field corrective actions Urgent Field Safety Notice for EndoFLIP System by Covidien llc 2026
- Reason
- assessment Field corrective actions Urgent Field Safety Notice for EndoFLIP System by Covidien llc 2026
- Classification
- Class I
- Category
- medical device recall
- Country
- Germany
- Agency
- BFARM
- Recall date
- 2026-05-19
- Status
- Ongoing
- Distribution
- Germany / EU
Official recall notice from BFARM
Recall details on Nibble Recalls: https://trynibble.app/recalls/304de50f-ea31-4920-b279-f2dbc4c5418b