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Urgent Safety Notice for Ingenia 1.5T and Ingenia 3T, Philips PDF, 96KB, File does not meet accessibility standards Date: 13. September 2011 Topics: Medical devices Type: Customer information

Product group Electromedical fields
Reference 04049/11

Important Safety Notice for MOSAIQ-Version 1.60V1 to v2.30.01, ELEKTA PDF, 196KB, File does not meet accessibility standards Date: 13. September 2011 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 03067/11

Recall of the device Philips NM3 Monitor, Respironics Deutschland GmbH PDF, 336KB, File does not meet accessibility standards Date: 12. September 2011 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 04104/11

Urgent Safety Notice for Lojer 200-Series treatment tables, Lojer OY PDF, 260KB, File does not meet accessibility standards Date: 12. September 2011 Topics: Medical devices Type: Customer information

Product group Physical therapy
Reference 03990/11

Recall for Vitros Chemistry Products PHBR Slides, Ortho Clinical Diagnostics PDF, 59KB, File does not meet accessibility standards Date: 12. September 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02910/11

Safety Notice concerning a corrective action of the radiotherapy planning system Eclipse version 10, Varian Medical Systems PDF, 338KB, File does not meet accessibility standards Date: 12. September 2011 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 03909/11

Recall for Dimension Vista CA19-9 Flex reagent cartridges, Siemens PDF, 86KB, File does not meet accessibility standards Date: 12. September 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 04020/11

Recall for CELLTRACKS Analyser II, Veridex PDF, 74KB, File does not meet accessibility standards Date: 12. September 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03910/11

Safety Notice for Etac Supportbelt / Etac Immedia Supportbelt A/S / Immedia A/S Supportbelt, Etac AB PDF, 296KB, File does not meet accessibility standards Date: 09. September 2011 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment
Reference 03373/11

Recall for the Aquamantis 2.3 Bipolar Sealer, Salient Surgical Technologies PDF, 33KB, File does not meet accessibility standards Date: 09. September 2011 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 03407/11

Lot Recall for the Corail AMT Size 9 und Size 10 Hip Implants, DePuy PDF, 96KB, File does not meet accessibility standards Date: 09. September 2011 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 03758/11

Lot Recall for DUET TRS Universal Straight and Articulating Single Use Loading Unit (SULU) PDF, 238KB, File does not meet accessibility standards Date: 08. September 2011 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 03889/11

Safety Notice concerning a corrective action of the AC 250 ISC Varian Proton Therapy Delivery System, Varian Medical Systems PDF, 774KB, File does not meet accessibility standards Date: 08. September 2011 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 03563/11

Safety Notice concerning a corrective action of the linear accelerator systems Hi Art, TomoTherapy Incorporated PDF, 38KB, File does not meet accessibility standards Date: 08. September 2011 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 03164/11

Lot Recall of a heart-lung bypass set intended for extracorporeal oxygenation, Maquet PDF, 656KB, File does not meet accessibility standards Date: 08. September 2011 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 02557/11

Recall for DiaSys respons 910 analyzer, DiaSys PDF, 528KB, File does not meet accessibility standards Date: 08. September 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03926/11

Recalls of certain ON-Q-Pumps with Select-A-Flow passive infusion pumps, Flow Corporation PDF, 2MB, File does not meet accessibility standards Date: 07. September 2011 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 03920/11

Field Safety Notice concerning a corrective action of syngo Imaging XS radiologic picture archiving and communication system, Siemens Healthcare PDF, 2MB, File does not meet accessibility standards Date: 07. September 2011 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 03824/11

Field Safety Notice concerning a corrective action of the TruPort ceiling support systems, Trumpf Medizin Systeme GmbH & Co. KG PDF, 60KB, File does not meet accessibility standards Date: 06. September 2011 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 03820/11

Recall for certain sterile packages of OP-sets / individual sets, MaiMed GmbH PDF, 54KB, File is accessible Date: 05. September 2011 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 03413/11

Recall of several batches of Biatain Ag Non-adhesive Foam Dressings, Coloplast PDF, 141KB, File does not meet accessibility standards Date: 31. August 2011 Topics: Medical devices Type: Customer information

Product group Dressings / Pads
Reference 03585/11

Recall for Dimension Vista Cuvettes, Siemens PDF, 100KB, File does not meet accessibility standards Date: 31. August 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03856/11

Safety Notice concerning corrective actions for X-ray system VIDIX U (Universal Type), Tetenal PDF, 633KB, File does not meet accessibility standards Date: 31. August 2011 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 02151/11

Safety Notice concerning a corrective action of the Armboards for operation tables 10-380, 10-380-K and 10-387, Reison Medical PDF, 32KB, File does not meet accessibility standards Date: 31. August 2011 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 03775/11

Recall for cobas c pack large D-Dimer, Roche PDF, 49KB, File does not meet accessibility standards Date: 31. August 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03863/11

Safety Notice for the Philips Allura Xper systems and Allura CV20, Philips PDF, 546KB, File does not meet accessibility standards Date: 30. August 2011 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 03631/11

Safety Notice concerning a corrective action of the Magnetic Resonance Imaging System MSK 1.5T Extreme, GE Healthcare PDF, 39KB, File does not meet accessibility standards Date: 30. August 2011 Topics: Medical devices Type: Customer information

Product group Electromedical fields
Reference 03871/11

Lot Recall of Endosgel 11 ml, Farco-Pharma PDF, 863KB, File does not meet accessibility standards Date: 30. August 2011 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 02983/11

Recall for the Immage Immunochemistry Systems Rheumatoid Factor (RF) Reagent, Beckman Coulter PDF, 250KB, File does not meet accessibility standards Date: 29. August 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02749/11

Recall for the Manual Inhibin A Elisa Reagent Kit, Beckman Coulter PDF, 46KB, File does not meet accessibility standards Date: 29. August 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03789/11