Urgent Field Safety Notice For Erytra By Diagnostic Grifols Sa

ERYTRA Field Safety Notice Diagnostic Grifols SA has issued a Class I urgent field safety notice for ERYTRA devices distributed in Germany and the EU. The notice indicates a serious problem with the device, though the specific reason is not detailed in the available information. This classification means the issue could result in serious injury or death.

Recalling firm
Diagnostic Grifols SA
Product
ERYTRA
Reason
Urgent Field Safety Notice for ERYTRA by Diagnostic Grifols SA
Classification
Class I
Category
medical device recall
Country
Germany
Agency
BFARM
Recall date
2026-07-30
Status
Ongoing
Distribution
Germany / EU

Official recall notice from BFARM

Recall details on Nibble Recalls: https://trynibble.app/recalls/95e750cb-8131-48de-9a9d-12a8821cb757