BfArM - Federal Institute for Drugs and Medical Devices

Navigation and service

Recall for Vitesse Biopsy needle, OptiMed

Product group Medical instruments for use in humans
Reference 02884/08

OptiMed Medizinische Instrumente GmbH recalls the lot number 6000017098 of the medical device Vitesse Biopsy needle, Ref 1399-1220. Due to a mistake a wrong needle with the diameter 1,6 mm was packed instead with the diameter 1,2 mm. Only the mentioned lot number is affected by the recall.

Recall for Vitesse Biopsy needle, OptiMed , Download_VeroeffentlichtAm_EN PDF, 120KB, File does not meet accessibility standards