BfArM - Federal Institute for Drugs and Medical Devices

Navigation and service

Lot recall of IMMULITE / 1000 Turbo D-Dimer assay, Siemens Healthcare Diagnostics Inc.

Product group In-vitro diagnostics - haematological, histological and cytological products
Reference 10348/16

For further information as well as details concerning the device please see the enclosed Advisory Notice of the manufacturer.

Lot recall of IMMULITE / 1000 Turbo D-Dimer assay, Siemens Healthcare Diagnostics Inc. , Download_VeroeffentlichtAm_EN PDF, 56KB, File does not meet accessibility standards

Use of cookies

Cookies help us to provide our services. By using our website you agree that we can use cookies. Read more about our Privacy Policy and visit the following link: Privacy Policy (only in German)

OK