BfArM - Federal Institute for Drugs and Medical Devices

Navigation and service

Corrective action/Recall for IMMULITE 2000 3gAllergy Specific IgE Universal Kit, Siemens

Product group In-vitro diagnostics
Reference 01934/10

Corrective action/Recall of Siemens for IMMULITE 2000 3gAllergy Specific IgE Universal Kit, L2KUN6 Lots 306, 307 and 308 because of incorrect calibration curve information detailed in the kit barcode. The customers were informed about the problem and how to avoid it.

Corrective action/Recall for IMMULITE 2000 3gAllergy Specific IgE Universal Kit, Siemens , Download_VeroeffentlichtAm_EN PDF, 24KB, File does not meet accessibility standards