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Lot Recall for handles, Rolko Kohlgrüber GmbH PDF, 68KB, File does not meet accessibility standards Date: 14. April 2010 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment
Reference 04313/09

Recall for EV1000 system with software version 0.1.1.52, Edwards Lifesciences PDF, 64KB, File does not meet accessibility standards Date: 14. April 2010 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 01198/10

Recall for Dimension Vista LOCI Reaction Vessel, Siemens PDF, 29KB, File does not meet accessibility standards Date: 13. April 2010 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01213/10

Recall for ETI-ANA Screen Catalog – N0093, DiaSorin PDF, 71KB, File does not meet accessibility standards Date: 13. April 2010 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 00910/10

Safety Notice for Innova 2100IQ, 3100IQ and 4100IQ, GE Healthcare PDF, 127KB, File does not meet accessibility standards Date: 13. April 2010 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 01150/10

Corrective action for Clinical Chemistry Total Bilirubin, Abbott PDF, 373KB, File does not meet accessibility standards Date: 12. April 2010 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02498/09

Security advice for Revitan Disassembly Instruments, Zimmer PDF, 157KB, File does not meet accessibility standards Date: 12. April 2010 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 01133/10

Lot Recall for Continium™ Acetabular Systems Shell Inserter Adapter with and without Rotational Control, Zimmer Inc. PDF, 246KB, File does not meet accessibility standards Date: 12. April 2010 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 01149/10

Recall for chloride electrodes for Advia Clinical Chemistry Systems, Siemens PDF, 66KB, File does not meet accessibility standards Date: 12. April 2010 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01116/10

Safety Information for corpuls3 defibrillator/monitoring system, GS Elektromedizinische Geräte G. Stemple GmbH PDF, 446KB, File does not meet accessibility standards Date: 09. April 2010 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 02035/09

Safety Notice for FRED easy, Schiller PDF, 79KB, File does not meet accessibility standards Date: 09. April 2010 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 02434/08

Urgent Safety Notice for Intracranial Stent "SILK", Balt PDF, 78KB, File does not meet accessibility standards Date: 09. April 2010 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 00938/10

Safety Notice for Calcuson Ultrasonic Generator / Endomat LC, Karl Storz GmbH & Co. KG PDF, 296KB, File does not meet accessibility standards Date: 09. April 2010 Topics: Medical devices Type: Customer information

Product group Ultrasonics
Reference 03724/09

Information for SERVO-i Ventilator System, Maquet PDF, 88KB, File does not meet accessibility standards Date: 07. April 2010 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 01709/09

Corrective Action for i-STAT Hematocrit/HCT and Calculated Hemoglobin/HB Cartridge and Test Information Sheets, Abbott PDF, 111KB, File does not meet accessibility standards Date: 06. April 2010 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 00578/10

Corrective action for Olympus PK7200 Blood Grouping Systems, Beckman Coulter PDF, 128KB, File does not meet accessibility standards Date: 06. April 2010 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 00729/10

Corrective Action for Triage TOX Drug Screen, Biosite PDF, 117KB, File does not meet accessibility standards Date: 06. April 2010 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 00944/10

Corrective action: 14.8-Volt Lithium Ion Battery for use with the Philips HeartStart MRx Monitor/Defibrillator, Philips PDF, 128KB, File does not meet accessibility standards Date: 01. April 2010 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 01034/10

Corrective Action/Recall for UniCel DxH 800 Coulter Cellular Analysis System, Beckman Coulter PDF, 58KB, File does not meet accessibility standards Date: 01. April 2010 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01028/10

Lot Recall for Flow Selector PM1000, Precision Medical Inc. PDF, 97KB, File does not meet accessibility standards Date: 01. April 2010 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 01000/10

Lot Recall for QWIX Bone Screws, Newdeal PDF, 75KB, File does not meet accessibility standards Date: 01. April 2010 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 00430/10

Additional Information for INFusor and FOLFusor pumps, Baxter PDF, 78KB, File does not meet accessibility standards Date: 31. March 2010 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 02802/09

Recall for Aneroid Sphygmomanometer Stethoscope, Wenzhou Bokang Instruments Co., Ltd Date: 31. March 2010 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment
Reference 04599/09

Safety Notice for Oncentra Brachy, Nucletron PDF, 499KB, File does not meet accessibility standards Date: 31. March 2010 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 00973/10

Lot Recall of a Tubing set for Blood Purification, Naniwa Rubber Co. Ltd. PDF, 61KB, File does not meet accessibility standards Date: 31. March 2010 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 00881/10

Recall of the 3,2mm Guide Pin Sleeve, Smith & Nephew Inc. PDF, 47KB, File does not meet accessibility standards Date: 31. March 2010 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 00623/10

Safety Notice for Axiom Artis, Siemens PDF, 69KB, File does not meet accessibility standards Date: 30. March 2010 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 00742/10

Safety Notice for radiotherapy treatment planning software iPlan RT Dose, BrainLab PDF, 77KB, File does not meet accessibility standards Date: 30. March 2010 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 00919/10

Safety Notice for SpineCath & Acutherm Catheters with Introducer Needles, Smith & Nephew PDF, 98KB, File does not meet accessibility standards Date: 30. March 2010 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 03466/08

Recall for Dyonics 25 Tube Sets, Smith&Nephew PDF, 34KB, File does not meet accessibility standards Date: 30. March 2010 Topics: Medical devices Type: Customer information

Product group Optics / Precision engineering
Reference 01002/10