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Extension of the recall of certain lots of the Mach I™ Guide Catheters from Boston Scientific PDF, 304KB, File does not meet accessibility standards Date: 12. September 2007 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 02557/07

Recall of the Colorado 2 Locking Nuts from Medtronic PDF, 231KB, File does not meet accessibility standards Date: 12. September 2007 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 03170/07

Recall of the resorbable bone screws Calaxo from Smith & Nephew PDF, 40KB, File does not meet accessibility standards Date: 12. September 2007 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 03129/07

Corrective action of the Infinity™ Ammonia Liquid Stable Reagent from Thermo Fisher Scientific PDF, 246KB, File does not meet accessibility standards Date: 12. September 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02871/07

Recall of the guide wires from C.R. Bard GmbH PDF, 78KB, File does not meet accessibility standards Date: 12. September 2007 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 03101/07

Recall for ABL77 cal pack lots from Radiometer Copenhagen PDF, 30KB, File does not meet accessibility standards Date: 11. September 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03100/07

Recall for the Data Innovations Instrument Manager from Beckman Coulter PDF, 171KB, File does not meet accessibility standards Date: 11. September 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03142/07

Recall for the IGF-I IRMA Kit from Beckman Coulter PDF, 38KB, File does not meet accessibility standards Date: 11. September 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03140/07

Recall of the Pressure transducers DPT 8003 from Codan pvb Critical Car GmbH PDF, 35KB, File does not meet accessibility standards Date: 11. September 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02994/07

Recall for the Trinity Biotech Captia Varicella-Zoster (VZV) IgM from Trinity Biotech PDF, 58KB, File does not meet accessibility standards Date: 10. September 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02379/07

Corrective action for the Strep A Schnelltest-Streifen and the Strep A Schnelltest-Gerät from Innovacon PDF, 50KB, File does not meet accessibility standards Date: 10. September 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02577/07

Safety Information concerning the pediatric fitting of hearing instruments INTUIS S Dir and CIELO 2 from Siemens Audiologische Technik GmbH PDF, 44KB, File does not meet accessibility standards Date: 10. September 2007 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 02648/07

Recall of Caeruloplasmin NL BINDARID Radial Immunodiffusion Kits from The Binding Site PDF, 112KB, File does not meet accessibility standards Date: 07. September 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02922/07

Recall of burs, irrigation instruments etc. from ConMed Linvatec PDF, 322KB, File does not meet accessibility standards Date: 06. September 2007 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 02915/07

Information about defective sterile packaging of OP sets („Procedure packs“) from Cardinal Health Germany PDF, 48KB, File does not meet accessibility standards Date: 05. September 2007 Topics: Medical devices Type: Customer information

Product group Dressings / Pads
Reference 02815/07

Recall of specifiy lot numbers of the infusion device Coventry Valve Triple IV Peripheral Connector Set from the manufacturer Mediplus Ltd. PDF, 667KB, File does not meet accessibility standards Date: 04. September 2007 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 02821/07

Information about the correct use of the EOLE battery pack from ResMed PDF, 86KB, File does not meet accessibility standards Date: 04. September 2007 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 03049/07

Information about Terumo Advanced Perfusion System 1 - Small Roller Pump and Large Roller Pump - from Terumo Cardiovascular Systems Corp. PDF, 98KB, File does not meet accessibility standards Date: 03. September 2007 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 02678/07

Recall of the products „ML Taper Offset Rasp Handle“ from Zimmer Inc., USA PDF, 66KB, File does not meet accessibility standards Date: 03. September 2007 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 02510/07

Information about pelvic belt at the Invacare Rea wheelchairs of the company Invacare Aquatec PDF, 24KB, File does not meet accessibility standards Date: 31. August 2007 Topics: Medical devices Type: Customer information

Product group Orthopaedic / Rehabilitation technology
Reference 02276/07

Information concerning dysfunctions with the 220-240 V base of the Terumo Advanced Perfusion System 1 of Terumo Cardiovascular Systems PDF, 131KB, File does not meet accessibility standards Date: 31. August 2007 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 02679/07

New Information about Lifepak CR Plus and Lifepak Express defibrillators of the manufacturer Medtronic GmbH PDF, 46KB, File does not meet accessibility standards Date: 30. August 2007 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 00789/07

Information for users of electro-surgery generators Electrotom 530, 621, 630, 640 and HITT 106 of the company Integra LifeSciences Services PDF, 122KB, File does not meet accessibility standards Date: 30. August 2007 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 02643/07

Recall for Dimension Total Bilirubin (TBIL) Flex reagent cartridge (Lot-Number FC8170) of Dade Behring PDF, 29KB, File does not meet accessibility standards Date: 29. August 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02987/07

Corrective action and recall for Dimension RxL Max / Xpand Plus Software Version 7.4 und QCC Power Pak of Dade Behring PDF, 25KB, File does not meet accessibility standards Date: 29. August 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02988/07

Corrective action for Multifibren U on BCS and BCS XP Systems of Dade Behring PDF, 39KB, File does not meet accessibility standards Date: 28. August 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02287/07

Information about a software update of Acuson Antares and Sonoline Antares ultrasound devices of Siemens PDF, 128KB, File does not meet accessibility standards Date: 28. August 2007 Topics: Medical devices Type: Customer information

Product group Ultrasonics
Reference 02959/07

Corrective action for vancomycin, valproinic acid and tobramycin tests on Cobas C501 and Modular Analytics P analyzers of Roche PDF, 66KB, File does not meet accessibility standards Date: 27. August 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01423/07

Information concerning an update of the WaveScan WaveFront software to version 3.671 from Advanced Medical Optics, Inc. PDF, 75KB, File does not meet accessibility standards Date: 27. August 2007 Topics: Medical devices Type: Customer information

Product group ophthalmological technology
Reference 02179/07

Corrective action for the FC 500 with CXP Acquisition Software of Beckman Coulter PDF, 45KB, File does not meet accessibility standards Date: 27. August 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02936/07