BfArM - Federal Institute for Drugs and Medical Devices

Navigation and service

Recall for Auto D Dimer Kit, Trinity Biotech

Product group In-vitro diagnostics
Reference 03007/09

Recall of Trinity Biotech for the Auto D Dimer Kit (Lot-No. T082003, T084001 und T119006) due to an erroneous calibration and falsely negative test results. Customers were advised to discard the affected batch.

Recall for Auto D Dimer Kit, Trinity Biotech , Download_VeroeffentlichtAm_EN PDF, 135KB, File does not meet accessibility standards