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Urgent Safety Notice for the product S4 Dynamic Rod, AESCULAP AG PDF, 309KB, File does not meet accessibility standards Date: 30. January 2014 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 00094/14

Safety Notice for the Cavitron® Inserts, DENTSPLY DETREY GmbH PDF, 1MB, File does not meet accessibility standards Date: 30. January 2014 Topics: Medical devices Type: Customer information

Product group Ultrasonics - ultrasonic equipment forf dentistry
Reference 05118/12

Recall for the Knot Pusher, Arthrocare PDF, 52KB, File does not meet accessibility standards Date: 30. January 2014 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 00265/14

Safety Notice for the MRP-TITAN and the KAM-Titan instruments, Peter Brehm GmbH PDF, 217KB, File does not meet accessibility standards Date: 30. January 2014 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 00147/14

Corrective action for cobas® PCR media, Roche PDF, 129KB, File does not meet accessibility standards Date: 29. January 2014 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - instruments, apparatuses and systems
Reference 07996/13

Urgent Safety Notice for the balanSys® Knee System, Mathys PDF, 533KB, File does not meet accessibility standards Date: 29. January 2014 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 00250/14

Urgent Safety Notice for Patient Monitors B20 / B40 V1, B30 and B40 V2, GE Healthcare PDF, 144KB, File does not meet accessibility standards Date: 29. January 2014 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrotherapy
Reference 07961/13

Lot Recall of Sandel Weighted Safety Scapels, Ansell Sandel Medical Solutions PDF, 274KB, File does not meet accessibility standards Date: 29. January 2014 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - general instruments
Reference 07625/13

Corrective action of the Powerheart G5 Automatic External Defibrillators (AEDs), Cardiac Science PDF, 131KB, File does not meet accessibility standards Date: 29. January 2014 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrotherapy
Reference 00261/14

Corrective action for bioNexia FOBplus, bioMérieux PDF, 46KB, File does not meet accessibility standards Date: 29. January 2014 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 00101/14

Lot Recall of Compoglass F, IVOCLAR VIVADENT PDF, 134KB, File does not meet accessibility standards Date: 29. January 2014 Topics: Medical devices Type: Customer information

Product group Dental products - dental material
Reference 00137/14

Recall for the single breathing hose system ClevAir, MPV Medical GmbH PDF, 102KB, File does not meet accessibility standards Date: 28. January 2014 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - anaesthesia and medical gas supply
Reference 08051/13

Safety Notice for the 15 L Cycler Drainage Bag, Baxter PDF, 141KB, File does not meet accessibility standards Date: 28. January 2014 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - dialysis technology
Reference 07927/13

Safety Notice for PLUM LifeCare™ 5000 Infusers, Hospira Inc. PDF, 2MB, File does not meet accessibility standards Date: 28. January 2014 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - infusion technology
Reference 07629/13

Safety Notice for Carescape Monitor B650 and B850, GE Healthcare Finland Oy PDF, 110KB, File does not meet accessibility standards Date: 28. January 2014 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrodiagnostics
Reference 00188/14

Urgent Safety Notice for the Zimmer Trabecular Metal™ Reverse Shoulder System Glenosphere & Base Plate, Zimmer Inc. PDF, 681KB, File does not meet accessibility standards Date: 28. January 2014 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 00170/14

Recall of several batches of the product Spiked Biopsy Forceps, Micro-Tech PDF, 42KB, File does not meet accessibility standards Date: 28. January 2014 Topics: Medical devices Type: Customer information

Product group Optics / Precision engineering - endoscopes
Reference 06984/13

Recall of one batch of the product M-flex intraocular lens, Rayner PDF, 1MB, File does not meet accessibility standards Date: 27. January 2014 Topics: Medical devices Type: Customer information

Product group Non-active implants - special implants
Reference 00117/14

Corrective action for SD Bioline Tetanus, Standard Diagnostics PDF, 560KB, File does not meet accessibility standards Date: 27. January 2014 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - immunological products
Reference 06933/13

Corrective action for BBL Staphyloslide Latex Test Kit, Becton Dickinson PDF, 45KB, File does not meet accessibility standards Date: 27. January 2014 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - microbiological products
Reference 00084/14

Corrective action from for Estrogen Receptor Ab-11, Thermo Fisher PDF, 148KB, File does not meet accessibility standards Date: 27. January 2014 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - immunological products
Reference 07084/13

Safety Notice concerning the List Mode Replay of the PET Discovery 610 and Discovery 710, PET Discovery 600 and Discovery 690. PDF, 107KB, File does not meet accessibility standards Date: 24. January 2014 Topics: Medical devices Type: Customer information

Product group Electromedical fields - equipment for MR tomography
Reference 07638/13

Another Safety Notice for the ACUSON SC2000, Siemens PDF, 564KB, File does not meet accessibility standards Date: 24. January 2014 Topics: Medical devices Type: Customer information

Product group Ultrasonics - ultrasonic diagnostic equipment
Reference 00154/14

Urgent Safety Notice for the ACUSON 802000™ ultrasound systems, Siemens PDF, 7MB, File does not meet accessibility standards Date: 24. January 2014 Topics: Medical devices Type: Customer information

Product group Ultrasonics - ultrasonic diagnostic equipment
Reference 00140/14

Urgent Safety Notice for the Philips BrightView SPECT, BrightView X and BrightView XCT Imaging Systems, Philips Healthcare PDF, 208KB, File does not meet accessibility standards Date: 24. January 2014 Topics: Medical devices Type: Customer information

Product group Radiological technology - CT scanners
Reference 00119/14

Recall of Adaptateur pour Flacon Isopack, Baxter Healthcare PDF, 115KB, File does not meet accessibility standards Date: 24. January 2014 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - syringes and cannulas
Reference 00082/14

Urgent Safety Notice for the extension device (“Raumextensionsgerät”), Lautenschläger PDF, 747KB, File does not meet accessibility standards Date: 24. January 2014 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 00054/14

Safety Notice for CEM™ Nosecones for use with CUSA® Excel/Excel+ Ultrasonic Aspirator, Integra LifeSciences PDF, 218KB, File does not meet accessibility standards Date: 24. January 2014 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrotherapy
Reference 07924/13

Safety Notice for the BD Plastipak™ 50ml Luer Lok Syringes with Syringe Pumps, Becton Dickinson PDF, 92KB, File does not meet accessibility standards Date: 24. January 2014 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - syringes and cannulas
Reference 00079/14

Recall TeleCare Monitor (TCM) 3370 / 3371, vitaphone GmbH PDF, 1MB, File does not meet accessibility standards Date: 24. January 2014 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrodiagnostics
Reference 08162/13