Urgent Field Safety Notice For Orbis Medication By Dh Healthcare Gmbh

ORBIS Medication Recall Summary DH Healthcare GmbH is recalling ORBIS Medication devices distributed in Germany and the EU due to an urgent safety concern. This is classified as a Class I recall, indicating a serious issue. The recall affects all users of this medication device in the affected regions.

Recalling firm
DH Healthcare GmbH
Product
ORBIS Medication
Reason
Urgent Field Safety Notice for ORBIS Medication by DH Healthcare GmbH
Classification
Class I
Category
medical device recall
Country
Germany
Agency
BFARM
Recall date
2026-07-14
Status
Ongoing
Distribution
Germany / EU

Official recall notice from BFARM

Recall details on Nibble Recalls: https://trynibble.app/recalls/9a3a69fc-59e3-4297-9208-769bd4665ebe