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14,972 results

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Lot recall of ARCHITECT Active-B12 Reagent Kit, Abbott PDF, 26KB, File does not meet accessibility standards Date: 21. December 2016 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 10481/16

Urgent field safety notice for ORTHO VISION® Analyzers with software version 3.6.0 and below, Ortho-Clinical Diagnostics PDF, 827KB, File does not meet accessibility standards Date: 21. December 2016 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 10546/16

Urgent field safety notice for Human Milk Analyser, MIRIS AB PDF, 138KB, File does not meet accessibility standards Date: 20. December 2016 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - instruments, apparatuses and systems
Reference 05011/16

Urgent field safety notice for PreciControl Varia, Level 2 - Elecsys® PTH assay on Elecsys® 2010 / cobas e 411, Roche Diagnostics GmbH PDF, 150KB, File does not meet accessibility standards Date: 20. December 2016 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 01724/16

Urgent field safety notice for QuikRead FOB Sampling-Set / QuikRead FOB quantitativ-Kit and QuikRead go iFOBT-Kit, Orion Diagnostika PDF, 97KB, File does not meet accessibility standards Date: 20. December 2016 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 10737/16

Urgent field safety notice for Source Administration Sets (SAS) used with the Medrad® Intego PET Infusion System (Catalog Number INT CSS), Bayer Medical Care Inc. PDF, 102KB, File does not meet accessibility standards Date: 19. December 2016 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - infusion technology
Reference 09575/16

Lot recall of position headed reamer scaled D8.0mm, Aesculap AG PDF, 59KB, File does not meet accessibility standards Date: 19. December 2016 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 11217/16

Recall of Inpactor for PFNA Blade, DePuy Synthes PDF, 87KB, File does not meet accessibility standards Date: 19. December 2016 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 11203/16

Lot recall of Screwdriver handle/ T-shape/ cannulated, Zimmer Biomet PDF, 190KB, File does not meet accessibility standards Date: 19. December 2016 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 11202/16

Lot recall of K-wire Ø1,2 mm L100 mm trocar tip non-sterile, Biotech Ortho / Wright PDF, 164KB, File does not meet accessibility standards Date: 16. December 2016 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 10411/16

Urgent field safety notice for instruments and containers: Java pedicle screw system / Fidji cervical / lumbar cage / Wallis posterior dynamic stabilization system, Zimmer Biomet PDF, 514KB, File does not meet accessibility standards Date: 16. December 2016 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 08875/16

Urgent field safety notice for Oxylog 3000 / plus, Drägerwerk AG & Co. KGaA PDF, 184KB, File does not meet accessibility standards Date: 15. December 2016 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - anaesthesia and medical gas supply
Reference 10717/16

Recall of Arthrex S3 Arm Sleeve Connector, Allen Medical / Hill-Rom SAS PDF, 169KB, File does not meet accessibility standards Date: 15. December 2016 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 11081/16

Urgent field safey notice for Atrium Ocean / Oasis / Express / Express Mini chest drainage products, Maquet Getinge Group PDF, 148KB, File does not meet accessibility standards Date: 15. December 2016 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - drainages and suction systems
Reference 10935/16

Batch recall of NewBreez intralaryngeal prosthesis, PROTiP Medical PDF, 108KB, File does not meet accessibility standards Date: 15. December 2016 Topics: Medical devices Type: Customer information

Product group Non-active implants - special implants
Reference 10585/16

Batch recall of sleep safe Sets, Fresenius Medical Care PDF, 148KB, File does not meet accessibility standards Date: 15. December 2016 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - dialysis technology
Reference 10618/16

Urgent field safety notice for CentraLink Data Management System, Siemens Healthcare Diagnostics Inc. PDF, 27KB, File does not meet accessibility standards Date: 15. December 2016 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrodiagnostics
Reference 10884/16

Urgent field safety notice for iPlan RT / iPlan RT Dose / BrainSCAN, Brainlab AG PDF, 407KB, File does not meet accessibility standards Date: 14. December 2016 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection - radiotherapy treatment planning systems
Reference 10947/16

Urgent field safety notice for Artis zee, Artis Q and Artis Q.zen, Siemens Healthcare GmbH PDF, 39KB, File does not meet accessibility standards Date: 13. December 2016 Topics: Medical devices Type: Customer information

Product group Radiological technology - radiological equipment for vascular diagnostics
Reference 10858/16

Urgent field safety notice for oneHbA1c IS, DiaSys Diagnostic Systems GmbH PDF, 149KB, File does not meet accessibility standards Date: 13. December 2016 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 10795/16

Lot recall of Titanium Bone Screws, Anton Hipp GmbH PDF, 410KB, File does not meet accessibility standards Date: 13. December 2016 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 10794/16

Urgent field safety notice for Heater cooler 1T / 3T / FlexTherm, Sorin Group Deutschland GmbH / LivaNova PLC PDF, 728KB, File does not meet accessibility standards Date: 09. December 2016 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 10412/16

Urgent field safety notice for cobas b 123 <3> and <4> system, Roche Diagnostics GmbH PDF, 240KB, File does not meet accessibility standards Date: 09. December 2016 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 09909/16

Urgent field safety notice for Heater Unit HCU 40, Maquet Cardiopulmonary GmbH PDF, 498KB, File does not meet accessibility standards Date: 09. December 2016 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 10216/16

Urgent field safety notice for Heater Unit HU 35, Maquet Cardiopulmonary GmbH PDF, 88KB, File does not meet accessibility standards Date: 09. December 2016 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 10216/16

Lot recall of Alegria Anti-Instrinsic Factor / Anti-Mycoplasma pneumoniae IgM Abs., Orgentec Diagnostika GmbH PDF, 47KB, File does not meet accessibility standards Date: 08. December 2016 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - microbiological products
Reference 10392/16

Recall of INRatio and INRatio 2 PT / INR Monitoring System, Alere PDF, 533KB, File does not meet accessibility standards Date: 08. December 2016 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - haematological, histological and cytological products
Reference 05802/16

Lot recall of i-PRF Tubes 10 mL, Process for PRF / ALL YOUNG PDF, 399KB, File does not meet accessibility standards Date: 07. December 2016 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - equipment for collecting blood products and peripheral stem cells
Reference Eudamed Reference: INC-FR-16-12-000066

Urgent field safety notice for Compact Suction Unit 4 (LCSU 4), Laerdal Medical AS PDF, 603KB, File does not meet accessibility standards Date: 07. December 2016 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 10610/16

Urgent field safety notice for ORTHO VISION Max / Analyzer for ORTHO BioVue Cassettes, Ortho Clinical Diagnostics PDF, 192KB, File does not meet accessibility standards Date: 07. December 2016 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 10194/16