BfArM - Federal Institute for Drugs and Medical Devices

Navigation and service

Corrective action and recall of Cepheid Europe for DX Software Smartcycler

Product group In-vitro diagnostics
Reference 01948/05

Corrective action and recall of Cepheid Europe for DX Software Smartcycler (Software versions 1.6, 1.7 and 1.7a) because of erroneous sample idendification and results. Customers were informed about the problem and how to avoid it. The affected software versions will be replaced by a new software.

Corrective action and recall of Cepheid Europe for DX Software Smartcycler , Download_VeroeffentlichtAm_EN PDF, 56KB,

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