Urgent Field Safety Notice For Dlp One-piece Pediatric Arterial Cannulae By Medtronic Inc
Recall Summary Medtronic is recalling DLP One-Piece Pediatric Arterial Cannulae (tubes used to access arteries in children) distributed in Germany and the EU due to a safety concern that has been classified as Class I, the most serious level. The specific reason for the recall is not clearly detailed in the available information. The recall affects pediatric patients who may have received this device.
- Recalling firm
- Urgent Field Safety Notice for DLP One-Piece Pediatric Arterial Cannulae by Medtronic Inc , Download_VeroeffentlichtAm_E
- Product
- s Tasks of the BfArM Risk assessment Field corrective actions Urgent Field Safety Notice for DLP One-Piece Pediatric Arterial Cannulae by Medtronic Inc 2026
- Reason
- assessment Field corrective actions Urgent Field Safety Notice for DLP One-Piece Pediatric Arterial Cannulae by Medtronic Inc 2026
- Classification
- Class I
- Category
- medical device recall
- Country
- Germany
- Agency
- BFARM
- Recall date
- 2026-06-10
- Status
- Ongoing
- Distribution
- Germany / EU
Official recall notice from BFARM
Recall details on Nibble Recalls: https://trynibble.app/recalls/16335421-a1fe-4e51-ade6-81b0a5d8e1e6