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Lot Recall of FLAMINGO Inflation Devices, Perouse Medical and B.Braun Melsungen AG PDF, 155KB, File does not meet accessibility standards Date: 11. April 2013 Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 01588/13

Safety Notice for the Avance CS2, GE Healthcare PDF, 59KB, File does not meet accessibility standards Date: 11. April 2013 Type: Customer information

Product group Surgical equipment/ Anaesthesia - anaesthesia and medical gas supply
Reference 00999/13

Safety Notice for “Maximo” hospital bed for children with the special design “washable”, Joh. Stiegelmeyer GmbH & Co. KG PDF, 2MB, File does not meet accessibility standards Date: 10. April 2013 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment
Reference 00078/13

Urgent Safety Notice for “Maximo” hospital bed for children, Joh. Stiegelmeyer GmbH & Co. KG PDF, 5MB, File does not meet accessibility standards Date: 10. April 2013 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment - furnishings
Reference 00078/13

Safety Notice for the products Z Hyalin Multipack, Z Hyalin Plus Multipack und Z Hyalcoat, Hyaltech Ltd. PDF, 3MB, File does not meet accessibility standards Date: 10. April 2013 Type: Customer information

Product group ophthalmological technology - liquid media for ophthalmological purposes
Reference 07366/12

Safety Notice for the Digital Mammography System AMULET f (FDR MS-2500), FUJIFILM PDF, 111KB, File does not meet accessibility standards Date: 10. April 2013 Type: Customer information

Product group Radiological technology - radiological equipment for mammographic diagnostics
Reference 01757/13

Lot Recall of the Connection Screw for PLATON Locking Nail, TANTUM PDF, 60KB, File does not meet accessibility standards Date: 09. April 2013 Type: Customer information

Product group Non-active implants - bone surgery
Reference 00011/13

Important Safety Information for the AeriSeal® System, AERIS THERAPEUTICS PDF, 2MB, File does not meet accessibility standards Date: 09. April 2013 Type: Customer information

Product group Non-active implants - special implants
Reference 01198/13

Recall of one lot of the Dilatator, De Bakey, Karl Leibinger GmbH PDF, 3MB, File does not meet accessibility standards Date: 09. April 2013 Type: Customer information

Product group Medical instruments for use in humans - vascular surgery
Reference 01231/13

Safety Notice for GemStar™ Infusion System, Hospira Inc. PDF, 724KB, File does not meet accessibility standards Date: 09. April 2013 Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - infusion technology
Reference 01263/13

Important Safety Notice for the Elekta Precise™ Tables, Elekta Ltd. PDF, 406KB, File does not meet accessibility standards Date: 09. April 2013 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection - others
Reference 01324/13

Safety Notice for GemStar™ Infusion System, Hospira Inc. PDF, 852KB, File does not meet accessibility standards Date: 09. April 2013 Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - infusion technology
Reference 01271/13

Lot Recall for the Medtronic Archer 0.035 inch (0.89 mm) Super Stiff Guidewire, Medtronic Inc. PDF, 86KB, File does not meet accessibility standards Date: 09. April 2013 Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 01294/13

Recall for a specific batch of the 55080D StarLock Instrument Adapter, Brainlab AG PDF, 812KB, File does not meet accessibility standards Date: 09. April 2013 Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 01598/13

Safety Notice for GemStar™-Infusion System, Hospira Inc. PDF, 697KB, File does not meet accessibility standards Date: 08. April 2013 Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - infusion technology
Reference 01264/13

Safety Notice for GemStar™-Infusion System, Hospira Inc. PDF, 707KB, File does not meet accessibility standards Date: 08. April 2013 Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - infusion technology
Reference 01284/13

Recall for OP-Sets with Neoject cannulas from the manufacturer Dispomed, 1stQ GmbH PDF, 605KB, File does not meet accessibility standards Date: 08. April 2013 Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - syringes and cannulas
Reference 01088/13

Corrective Action for Automated Hematology Analyzer XP-300, Sysmex PDF, 43KB, File does not meet accessibility standards Date: 08. April 2013 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - haematological, histological and cytological products
Reference 01282/13

Correction of the Instruction for Use for the Blue Free Strand Orthocord® Sutures, DePuy Synthes PDF, 96KB, File does not meet accessibility standards Date: 08. April 2013 Topics: Medical devices Type: Customer information

Product group Dressings / Pads - surgical sutures, vascular loops etc.
Reference 01715/13

Lot Recall of the Archer 0.035 inch (0.89mm) Super Stiff Guidewire, Medtronic Inc. PDF, 103KB, File does not meet accessibility standards Date: 05. April 2013 Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 01310/13

Safety Notice for LifeCare 4200 PCA Infusion System, Hospira Inc. PDF, 737KB, File does not meet accessibility standards Date: 05. April 2013 Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - infusion technology
Reference 00983/13

Lot Recall of ELS-Cannulas used for ECMO Therapy, MAQUET PDF, 985KB, File does not meet accessibility standards Date: 05. April 2013 Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 07890/12

Safety Information for the Surgical Technique Guide of the Midfoot Fusion Bolt, Synthes PDF, 72KB, File does not meet accessibility standards Date: 05. April 2013 Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 01234/13

Lot Recall of the Trocar catheter, P.J. Dahlhausen PDF, 953KB, File does not meet accessibility standards Date: 05. April 2013 Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - drainages and suction systems
Reference 00632/13

Recall of the Antecurved Femur resection Prosthesis (AFP), Chiropro PDF, 90KB, File does not meet accessibility standards Date: 04. April 2013 Type: Customer information

Product group Non-active implants - bone surgery
Reference 01315/13

Lot Recall for Twinfix Ultra Ti Suture Anchor, Smith & Nephew PDF, 121KB, File does not meet accessibility standards Date: 04. April 2013 Type: Customer information

Product group Non-active implants - bone surgery
Reference 04607/12

Lot Recall for Guardian II und Guardian II NC Hemostasis Valves, Vascular Solutions PDF, 122KB, File does not meet accessibility standards Date: 04. April 2013 Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 01078/13

Recall for the Nicolet™ EEG Wireless Amplifier, Natus Neurology Incorporated PDF, 2MB, File does not meet accessibility standards Date: 04. April 2013 Type: Customer information

Product group Medical electronics / Electromedical devices - electrodiagnostics
Reference 00915/13

Lot Recall for the Disposable Pressure Monitoring Kit with VAMP Plus System, Edwards Lifesciences PDF, 80KB, File does not meet accessibility standards Date: 03. April 2013 Type: Customer information

Product group Medical electronics / Electromedical devices - electronic blood pressure monitor
Reference 00471/13

Lot Recall for the MTP Fusion Plates, SYNTHES PDF, 736KB, File does not meet accessibility standards Date: 03. April 2013 Type: Customer information

Product group Non-active implants - bone surgery
Reference 01318/13