Urgent Field Safety Notice For Viacath Ng 4/s/5mm, Viacath 20/xl/2-8-2mm By Vascomed Gmbh
Recall Summary VascoMed GmbH is recalling ViaCath NG 4/S/5mm and ViaCath 20/XL/2-8-2mm catheters distributed in Germany and the EU. This is a Class I recall, meaning there is a serious risk of injury or death. The specific reason for the recall is not clearly stated in the document provided, but it prompted urgent corrective action by the manufacturer.
- Recalling firm
- Urgent Field Safety Notice for ViaCath NG 4/S/5mm, ViaCath 20/XL/2-8-2mm by VascoMed GmbH , Download_VeroeffentlichtAm_E
- Product
- s Tasks of the BfArM Risk assessment Field corrective actions Urgent Field Safety Notice for ViaCath NG 4/S/5mm, ViaCath 20/XL/2-8-2mm by VascoMed GmbH 2026
- Reason
- assessment Field corrective actions Urgent Field Safety Notice for ViaCath NG 4/S/5mm, ViaCath 20/XL/2-8-2mm by VascoMed GmbH 2026
- Classification
- Class I
- Category
- medical device recall
- Country
- Germany
- Agency
- BFARM
- Recall date
- 2026-05-15
- Status
- Ongoing
- Distribution
- Germany / EU
Official recall notice from BFARM
Recall details on Nibble Recalls: https://trynibble.app/recalls/02ccfcd0-6cc9-4cf3-814b-cbbf2e844001