BfArM - Federal Institute for Drugs and Medical Devices

Navigation and service

Recall of DiaPlastin from the manufacturer Diamed

Product group In-vitro diagnostics
Reference 01067/07

Recall of Diamed for DiaPlastin (lot numbers 30050.08.xx, 30050.09.xx, 30050.10.xx, 30050.11.xx, 30050.12.xx and 30050.13.xx) because of prolonged clotting times. Customers were informed to discard the affected batches. The German market is not affected by the corrective action.

Recall of DiaPlastin from the manufacturer Diamed , Download_VeroeffentlichtAm_EN

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