Urgent Field Safety Notice For Bobby 8f By Microvention Europe

Recall Summary MicroVention Europe has issued an urgent field safety notice for the BOBBY 8F device, which is classified as a Class I recall. The notice affects devices distributed in Germany and the EU, though the specific reason for the recall is not clearly detailed in the available information. This is a medical device recall requiring urgent attention from affected users or healthcare facilities.

Recalling firm

Urgent Field Safety Notice for BOBBY 8F by MicroVention Europe , Download_VeroeffentlichtAm_EN 2026.04.29 PDF, 445KB, Fi

Product

s Tasks of the BfArM Risk assessment Field corrective actions Urgent Field Safety Notice for BOBBY 8F by MicroVention Europe 2026

Reason

assessment Field corrective actions Urgent Field Safety Notice for BOBBY 8F by MicroVention Europe 2026

Classification

Class I

Category

medical device recall

Country

Germany

Agency

BFARM

Recall date

2026-04-29

Status

Ongoing

Distribution

Germany / EU

Official recall notice from BFARM

Recall details on Nibble Recalls: https://trynibble.app/recalls/234b9880-9c8d-44ce-a509-b06c4ac3a534