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Lot Recall of the Triathlon Size 3-6 PS Femoral & Tibial Trialing Lower Tray, Stryker PDF, 144KB, File does not meet accessibility standards Date: 24. July 2013 Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 03851/13

Synthes GmbH: Lot Recall of the Bending Irons for Rods 5.5 mm, left and right, for Coronal Plane PDF, 531KB, File does not meet accessibility standards Date: 24. July 2013 Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 03592/13

Batch Recall of Winged Surecan Needles, B. Braun Medical PDF, 466KB, File does not meet accessibility standards Date: 24. July 2013 Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - syringes and cannulas
Reference 04066/13

Another Safety Notice concerning Series Unique Identifier (UID) issue associated with MR products, GE Healthcare PDF, 66KB, File does not meet accessibility standards Date: 24. July 2013 Topics: Medical devices Type: Customer information

Product group Electromedical fields
Reference 02864/13

Safety Notice concerning Series Unique Identifier (UID) issue associated with MR products, GE Healthcare PDF, 65KB, File does not meet accessibility standards Date: 24. July 2013 Topics: Medical devices Type: Customer information

Product group Electromedical fields - equipment for MR tomography
Reference 02864/13

Lot Recall for the BE-ECLS 2.8 Set, MAQUET Cardiopulmonary AG PDF, 429KB, File does not meet accessibility standards Date: 23. July 2013 Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 03577/13

Lot Recall for Lightspeed LSX Files, SYBRON PDF, 170KB, File does not meet accessibility standards Date: 23. July 2013 Topics: Medical devices Type: Customer information

Product group Dental products - instruments
Reference 01164/13

Safety Notice for Digital Accelerators with Electrons and Beam Modulator, MLCi/MLCi2, Agility or Asymmetric Heads, Elekta PDF, 129KB, File does not meet accessibility standards Date: 23. July 2013 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection - radiation facilites with accelerators for teletherapy
Reference 03400/13, 03406/13

Lot Recall for the sinus-XL Stent, OptiMed PDF, 866KB, File does not meet accessibility standards Date: 23. July 2013 Type: Customer information

Product group Non-active implants - special implants
Reference 03651/13

Corrective action for BD™ Stem Cell Control Kit, Becton Dickinson PDF, 66KB, File does not meet accessibility standards Date: 23. July 2013 Type: Customer information

Product group In-vitro diagnostics - haematological, histological and cytological products
Reference 03399/13

Important Safety Notice concerning the Co-Pilot Attendant Control P+ and R-net, Permobil PDF, 69KB, File does not meet accessibility standards Date: 22. July 2013 Type: Customer information

Product group Orthopaedic / Rehabilitation technology - mobility aids
Reference 03244/13

Safety Notice for the Frameless SRS QA Target Pointer, Brainlab AG PDF, 83KB, File does not meet accessibility standards Date: 22. July 2013 Type: Customer information

Product group Radiotherapy / Radiation protection - others
Reference 03954/13

Corrective action for TSKgel G8 β-Thal. HSi, Tosoh Bioscience PDF, 133KB, File does not meet accessibility standards Date: 22. July 2013 Type: Customer information

Product group In-vitro diagnostics - instruments, apparatuses and systems
Reference 03494/13

Safety Notice for the V60 Ventilator, Respironics California PDF, 170KB, File does not meet accessibility standards Date: 22. July 2013 Type: Customer information

Product group Surgical equipment/ Anaesthesia - anaesthesia and medical gas supply
Reference 03530/13

Safety Notice for Nihon Kohden Telemetry Systems WEP-5204K, WEP-5208K using Software Version ≤ 03-10 PDF, 123KB, File does not meet accessibility standards Date: 22. July 2013 Type: Customer information

Product group Medical electronics / Electromedical devices - electrodiagnostics
Reference 04024/13

Lot Recall of the product CELT ACD (6F) Femoral Artery Vascular Closure Device, Vasorum Ltd. PDF, 404KB, File does not meet accessibility standards Date: 22. July 2013 Topics: Medical devices Type: Customer information

Product group Non-active implants - special implants
Reference 03705/13

Lot Recall of the CHEX Circular Stapler, Frankenman International Limited PDF, 113KB, File does not meet accessibility standards Date: 22. July 2013 Type: Customer information

Product group Medical instruments for use in humans - general instruments
Reference 02875/13

Corrective action for Dimension Vista 500® and Dimension® Vista 1500, Siemens PDF, 30KB, File does not meet accessibility standards Date: 18. July 2013 Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 03107/13

Corrective action for FSH One Step Menopause Test Device (Urine), Innovacon PDF, 416KB, File does not meet accessibility standards Date: 18. July 2013 Type: Customer information

Product group In-vitro diagnostics - immunological products
Reference 03729/13

Recall of the GENESIS II Cruciate Retaining Insert Trials, Smith & Nephew PDF, 53KB, File does not meet accessibility standards Date: 18. July 2013 Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 03877/13

Corrective action for IH-1000, Bio-Rad Laboratories PDF, 914KB, File does not meet accessibility standards Date: 18. July 2013 Type: Customer information

Product group In-vitro diagnostics - haematological, histological and cytological products
Reference 02866/13

Lot Recall of the 27 G disposable cannula provided with the Amvisc® und Amvisc® Plus viscoelastic devices, Bausch & Lomb PDF, 2MB, File does not meet accessibility standards Date: 18. July 2013 Topics: Medical devices Type: Customer information

Product group ophthalmological technology - liquid media for ophthalmological purposes
Reference 07483/12

Corrective action for the Multidrogen Speicheltest, Ökonomed PDF, 32KB, File does not meet accessibility standards Date: 18. July 2013 Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 03829/13

Recall of Hand pendants for OPERON D 850, D 820 und D 760 operating tables, Berchtold PDF, 75KB, File does not meet accessibility standards Date: 18. July 2013 Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 01227/13

Lot Recall for BioMend®, BioMend Extend™, CollaCote®, CollaPlug® and CollaTape®, INTEGRA PDF, 54KB, File does not meet accessibility standards Date: 18. July 2013 Topics: Medical devices Type: Customer information

Product group Dental products - others
Reference 03167/13

Safety Notice for the High Energy Clinacs®, Varian Medical Systems PDF, 92KB, File does not meet accessibility standards Date: 17. July 2013 Type: Customer information

Product group Radiotherapy / Radiation protection - radiation facilites with accelerators for teletherapy
Reference 03220/13

Lot Recall of the Gamma 3 Long Nail Kit, STRYKER PDF, 42KB, File does not meet accessibility standards Date: 17. July 2013 Type: Customer information

Product group Non-active implants - bone surgery
Reference 02763/13

Corrective action for Alegria Anti-Intrinsic Factor Assay, Orgentec Diagnostica PDF, 99KB, File does not meet accessibility standards Date: 17. July 2013 Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 03444/13

Urgent Safety Notice for the X Mobil patient positioning table, Roesys PDF, 783KB, File does not meet accessibility standards Date: 17. July 2013 Type: Customer information

Product group Radiological technology - stationary radiological equipment
Reference 02951/13

Lot Recall of the HLS arterial cannulas with Bioline coating, Maquet PDF, 388KB, File does not meet accessibility standards Date: 17. July 2013 Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 03261/13