BfArM - Federal Institute for Drugs and Medical Devices

Navigation and service

Search i

Search help

  • Enter one or more search terms in the search field. Upper and lower case are not relevant.
  • As soon as you have entered three letters in the search field, various search words will be suggested from which you can choose one.
  • If you are searching for a certain group of words, put these words in double quotes. The hits will then contain the words in the order you entered, e.g. "medicines for children".
  • Multiple search terms can also be combined with the Boolean operators AND and OR. When using the operator AND, the results contain the intersection of all search terms. When using the operator OR, the hits contain one of the search terms or only individual search terms. The result set is therefore significantly larger. Please note that these operators must be written in capital letters.
  • If you receive a (too) large number of hits as a result of your search, you can narrow it down by using filters. These filter options appear to the left of the search results and are subdivided into:

    • category (e.g. safety of medicinal products, medical devices, code systems)
    • format (e.g. download, risk information, DHPCs)
    • time interval (e.g. last 30 days, older than ...)
  • Selected filters can be removed individually or all at once ("Show all results").
  • By default, search results are sorted by relevance, but they can also be sorted chronologically ("Latest entries first" or "Oldest entries first").

Enter search term

15,455 results

Filter

Results per page: 10 20 30

Safety Notice concerning an update for mediCAD versions 2.50 and higher, Hectec GmbH PDF, 394KB, File does not meet accessibility standards Date: 21. February 2013 Type: Customer information

Product group Medical data processing (software) - others
Reference 05538/12

Lot Recall of the Neoject Cannula, Dispomed Witt PDF, 93KB, File does not meet accessibility standards Date: 21. February 2013 Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - syringes and cannulas
Reference 00666/13

Safety Information for patient hoses XD 2040, Ulrich GmbH & Co. KG PDF, 1MB, File does not meet accessibility standards Date: 21. February 2013 Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - infusion technology
Reference 05566/12

Recall for Drug Wipe 6 S, Securetec PDF, 124KB, File does not meet accessibility standards Date: 20. February 2013 Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 00055/13

Urgent Safety Notice about corrective actions for CT systems (listed below), Philips Healthcare PDF, 1MB, File does not meet accessibility standards Date: 20. February 2013 Type: Customer information

Product group Radiological technology - CT scanners
Reference 00308/13

Safety Notice for the ACUSON S2000 Automated Breast Volume Scanner, Siemens PDF, 106KB, File does not meet accessibility standards Date: 20. February 2013 Topics: Medical devices Type: Customer information

Product group Ultrasonics - ultrasonic diagnostic equipment
Reference 00484/13

Amendment to the recall (24.04.2012) for HemosIL von Willebrand Factor Activity, Instrumentation Laboratory PDF, 685KB, File does not meet accessibility standards Date: 20. February 2013 Type: Customer information

Product group In-vitro diagnostics - haematological, histological and cytological products
Reference 02381/12

Safety Notice for the Philips MobileDiagnost wDR, Philips Medical Systems PDF, 19KB, File does not meet accessibility standards Date: 20. February 2013 Type: Customer information

Product group Radiological technology - stationary radiological equipment
Reference 00139/13

Safety Notice for MX 16-Slice, MX 4000, MX 4000 Dual and MX 6000 CT systems, Philips Healthcare PDF, 2MB, File does not meet accessibility standards Date: 20. February 2013 Type: Customer information

Product group Radiological technology - CT scanners
Reference 00236/13

Extension of the Urgent Medical Device Notification for the Trilogy® Acetabular System, Zimmer PDF, 25KB, File does not meet accessibility standards Date: 19. February 2013 Type: Customer information

Product group Non-active implants - bone surgery
Reference 06219/12

Important Product Information for HomeChoice Automated PD System and HomeChoice PRO Automated PD System, Baxter PDF, 79KB, File does not meet accessibility standards Date: 19. February 2013 Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - dialysis technology
Reference 00303/13

Recall for the UCFP Flex reagent cartridge, Siemens PDF, 50KB, File does not meet accessibility standards Date: 19. February 2013 Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 07910/12

Recall for BD MAX PCR Cartridges, Beckton Dickinson PDF, 49KB, File does not meet accessibility standards Date: 19. February 2013 Type: Customer information

Product group In-vitro diagnostics - microbiological products
Reference 08010/12

Recall for the Confidence Spinal Cement System Kit, DEPUY PDF, 93KB, File does not meet accessibility standards Date: 19. February 2013 Type: Customer information

Product group Non-active implants - bone surgery
Reference 00366/13

Corrective Action for BD MAX (6 channel) Instrument, Becton Dickinson PDF, 53KB, File does not meet accessibility standards Date: 19. February 2013 Type: Customer information

Product group In-vitro diagnostics - instruments, apparatuses and systems
Reference 06509/12

Urgent Safety Notice concerning Gambro bloodlines, Gambro PDF, 1MB, File does not meet accessibility standards Date: 19. February 2013 Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - dialysis technology
Reference 00345/13

Corrective Action for Oxoid Staphytect plus 500 Test and Oxoid Staphytect plus 100, Oxoid PDF, 20KB, File does not meet accessibility standards Date: 18. February 2013 Type: Customer information

Product group In-vitro diagnostics - microbiological products
Reference 07335/12

Recall for MicroScan Pos BP Combo Type 28 Panels, Siemens PDF, 23KB, File does not meet accessibility standards Date: 18. February 2013 Type: Customer information

Product group In-vitro diagnostics - microbiological products
Reference 07976/12

Recall for Sofia Influenza A+B FIA, Quidel PDF, 12MB, File does not meet accessibility standards Date: 18. February 2013 Type: Customer information

Product group In-vitro diagnostics - microbiological products
Reference 07692/12

Corrective Action of Roche for COBAS b 123 Fluid Pack COOX, 200, 400, 700 PDF, 291KB, File does not meet accessibility standards Date: 18. February 2013 Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 06961/12

Corrective Action for cobas 8000 data manager, COBAS INTEGRA 400 and COBAS INTEGRA 400 plus, Roche PDF, 81KB, File does not meet accessibility standards Date: 18. February 2013 Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 06670/12

Lot Recall for ALLEVYN Cavity Wound 5 cm circular, Smith & Nephew PDF, 103KB, File does not meet accessibility standards Date: 18. February 2013 Topics: Medical devices Type: Customer information

Product group Dressings / Pads - dressings
Reference 00603/13

Corrective action for STA – Liatest VWF in combination with STA-R / STA-R Evolution, Roche PDF, 22KB, File does not meet accessibility standards Date: 15. February 2013 Type: Customer information

Product group In-vitro diagnostics - haematological, histological and cytological products
Reference 00378/13

Corrective Action for Antimicrobial Susceptibility Testing Disc VA5 Vancomycin, Oxoid PDF, 16KB, File does not meet accessibility standards Date: 15. February 2013 Type: Customer information

Product group In-vitro diagnostics - microbiological products
Reference 07430/12

Lot Recall for the angle-stable plates, AAP IMPLANTATE PDF, 170KB, File does not meet accessibility standards Date: 15. February 2013 Type: Customer information

Product group Non-active implants - bone surgery
Reference 00282/13

Recall for the RHK knee system, Biomet PDF, 3MB, File does not meet accessibility standards Date: 15. February 2013 Type: Customer information

Product group Non-active implants - bone surgery
Reference 07959/12

Recall for the ADEPT 12/14 MoM modular hip heads, DePuy International Ltd. PDF, 137KB, File does not meet accessibility standards Date: 15. February 2013 Type: Customer information

Product group Non-active implants - bone surgery
Reference 00404/13

Lot Recall for the Cone Separators, Stryker Orthopaedics PDF, 50KB, File does not meet accessibility standards Date: 15. February 2013 Type: Customer information

Product group Non-active implants - bone surgery
Reference 00032/13