Urgent Field Safety Notice For Endura, Pulsera, Vectra, Veradius, And Zenition By Philips Medical Systems Internatonal Bv
Recall Summary Philips Medical Systems has issued an urgent safety notice for five medical device models: Endura, Pulsera, Vectra, Veradius, and Zenition. The notice is classified as Class I, indicating a serious safety concern. These devices were distributed in Germany and the EU.
- Recalling firm
- Philips Medical Systems Internatonal BV
- Product
- Endura, Pulsera, Vectra, Veradius, and Zenition
- Reason
- Urgent Field Safety Notice for Endura, Pulsera, Vectra, Veradius, and Zenition by Philips Medical Systems Internatonal BV
- Classification
- Class I
- Category
- medical device recall
- Country
- Germany
- Agency
- BFARM
- Recall date
- 2026-08-27
- Status
- Ongoing
- Distribution
- Germany / EU
Official recall notice from BFARM
Recall details on Nibble Recalls: https://trynibble.app/recalls/166fd666-a48e-4bd8-8dc1-1b45545a264d