Urgent Field Safety Notice For Clinitek Novus By Siemens Healthcare Diagnostics Inc., Norwood

Clinitek Novus Recall Summary Siemens Healthcare Diagnostics Inc. has issued a Class I urgent field safety notice for the Clinitek Novus device, which is distributed in Germany and throughout the EU. The notice does not specify the underlying safety issue in the provided information. This classification indicates a serious problem that could cause harm or incorrect test results.

Recalling firm
Siemens Healthcare Diagnostics Inc., Norwood
Product
Clinitek Novus
Reason
Urgent Field Safety Notice for Clinitek Novus by Siemens Healthcare Diagnostics Inc., Norwood
Classification
Class I
Category
medical device recall
Country
Germany
Agency
BFARM
Recall date
2026-06-03
Status
Ongoing
Distribution
Germany / EU

Official recall notice from BFARM

Recall details on Nibble Recalls: https://trynibble.app/recalls/1f4254bb-73ab-40cc-a90b-94efde899af3