Urgent Field Safety Notice For Vue Pacs (diagnostic) V12, Vue Motion V12 By Philips Medical Systems Nederland B.v.
Recall Summary Philips Medical Systems has issued an urgent safety notice for Vue PACS (Diagnostic) V12 and Vue Motion V12 medical imaging software systems used in Germany and the EU. The notice is classified as Class I, the most serious category. The specific technical reason for the notice is not detailed in the available information.
- Recalling firm
- Philips Medical Systems Nederland B.V.
- Product
- Vue PACS (Diagnostic) V12, Vue Motion V12
- Reason
- Urgent Field Safety Notice for Vue PACS (Diagnostic) V12, Vue Motion V12 by Philips Medical Systems Nederland B.V.
- Classification
- Class I
- Category
- medical device recall
- Country
- Germany
- Agency
- BFARM
- Recall date
- 2026-09-02
- Status
- Ongoing
- Distribution
- Germany / EU
Official recall notice from BFARM
Recall details on Nibble Recalls: https://trynibble.app/recalls/0e409d1a-b18a-4a6f-8f9a-e1e8a3e23917