BfArM - Federal Institute for Drugs and Medical Devices

Navigation and service

Recall for the FOCUS Gesundheit Kinderwunsch-Test, ulti med Products (Deutschland) GmbH

Product group In-vitro diagnostics - immunological products
Reference 00830/13

For further information as well as details concerning the device please see the enclosed Advisory Notice of the manufacturer. According to the information of the manufacturer only German customers are affected.

Recall for the FOCUS Gesundheit Kinderwunsch-Test, ulti med Products (Deutschland) GmbH , Download_VeroeffentlichtAm_EN PDF, 213KB, 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