Urgent Field Safety Notice For Procedure Packs (akd Kitpack) By Lohmann Und Rauscher Gmbh & Co. Kg

Recall Summary Lohmann und Rauscher GmbH & Co. KG is issuing a Class I safety notice for AKD Kitpack procedure packs distributed in Germany and the EU. The specific reason for the recall is not clearly stated in the available information, but this is classified as an urgent field safety notice for medical devices. Healthcare facilities and users of these procedure packs in affected regions should be aware of this notice.

Recalling firm

Urgent Field Safety Notice for Procedure packs (AKD Kitpack) by Lohmann und Rauscher GmbH & Co. KG , Download_Veroeffent

Product

s Tasks of the BfArM Risk assessment Field corrective actions Urgent Field Safety Notice for Procedure packs (AKD Kitpack) by Lohmann und Rauscher GmbH & Co

Reason

assessment Field corrective actions Urgent Field Safety Notice for Procedure packs (AKD Kitpack) by Lohmann und Rauscher GmbH & Co

Classification

Class I

Category

medical device recall

Country

Germany

Agency

BFARM

Recall date

2026-05-05

Status

Ongoing

Distribution

Germany / EU

Official recall notice from BFARM

Recall details on Nibble Recalls: https://trynibble.app/recalls/6ce74c8e-23a3-4284-a0b8-b2c062c93ee1