Urgent Field Safety Notice For Loop By Olympus Europa S. & Co. Kg

Recall Summary LOOP by Olympus Europa medical devices are being recalled in Germany and the EU due to a safety concern classified as Class I, the most serious level. The recall affects devices distributed in these regions. Specific details about which LOOP products are included and the exact nature of the safety risk are not provided in the available information.

Recalling firm

Urgent Field Safety Notice for LOOP by OLYMPUS EUROPA S. & Co. KG , Download_VeroeffentlichtAm_EN 2026.05.06 PDF, 895KB,

Product

s Tasks of the BfArM Risk assessment Field corrective actions Urgent Field Safety Notice for LOOP by OLYMPUS EUROPA S

Reason

assessment Field corrective actions Urgent Field Safety Notice for LOOP by OLYMPUS EUROPA S

Classification

Class I

Category

medical device recall

Country

Germany

Agency

BFARM

Recall date

2026-05-06

Status

Ongoing

Distribution

Germany / EU

Official recall notice from BFARM

Recall details on Nibble Recalls: https://trynibble.app/recalls/a5ce7fa4-4bcd-4f52-81cb-4b2d6db6e2ca