Urgent Field Safety Notice For Allura Xper, Allura Centron, Allura Cv20, Md-eleva By Philips Medical Systems Nederland B.v

Recall Summary Philips Medical Systems is issuing an urgent field safety notice for four X-ray imaging systems: Allura Xper, Allura Centron, Allura CV20, and MD-Eleva. The notice is classified as Class I, indicating a serious safety issue, though the specific reason is not clearly detailed in the provided information. These medical devices are distributed in Germany and the EU.

Recalling firm

Urgent Field Safety Notice for Allura Xper, Allura Centron, Allura CV20, MD-Eleva by Philips Medical Systems Nederland B

Product

s Tasks of the BfArM Risk assessment Field corrective actions Urgent Field Safety Notice for Allura Xper, Allura Centron, Allura CV20, MD-Eleva by Philips Medical Systems Nederland B

Reason

assessment Field corrective actions Urgent Field Safety Notice for Allura Xper, Allura Centron, Allura CV20, MD-Eleva by Philips Medical Systems Nederland B

Classification

Class I

Category

medical device recall

Country

Germany

Agency

BFARM

Recall date

2026-05-26

Status

Ongoing

Distribution

Germany / EU

Official recall notice from BFARM

Recall details on Nibble Recalls: https://trynibble.app/recalls/c1664179-48b2-467d-8094-3f5136feba08