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Recall of the Chemosite System – Peel Away Sheath Introducer from Tyco Healthcare PDF, 122KB, File does not meet accessibility standards Date: 26. June 2006 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 01581/06

Recall of the Synergy Porous Femoral component by Smith & Nephew PDF, 88KB, File does not meet accessibility standards Date: 26. June 2006 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 01674/06

Recall of components of the Legion knee replacement from Smith & Nephew PDF, 65KB, File does not meet accessibility standards Date: 26. June 2006 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 01684/06

Warning for OMNEX Surgical Sealant from the company Ethicon PDF, 83KB, File does not meet accessibility standards Date: 23. June 2006 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 01587/06

Recall of the Journey Quick Connect T-Handles from Smith & Nephew PDF, 83KB, File does not meet accessibility standards Date: 23. June 2006 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 01663/06

Corrective action for AxSYM analyzers from Abbott PDF, 276KB, File does not meet accessibility standards Date: 22. June 2006 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01652/06

Recall of NPT7 cartridges, Radiometer PDF, 30KB, File does not meet accessibility standards Date: 22. June 2006 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01257/06

Information for the ABSOLUTE™ .035 Peripheral Stents from Abbott PDF, 125KB, File does not meet accessibility standards Date: 22. June 2006 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 00952/06

Recall of the suture Sulene from Serag-Wiessner PDF, 154KB, File does not meet accessibility standards Date: 21. June 2006 Topics: Medical devices Type: Customer information

Product group Dressings / Pads
Reference 01495/06

Recall of High Flow Blood/Fluid Disposable Sets from Arizant PDF, 228KB, File does not meet accessibility standards Date: 21. June 2006 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 01459/06

Information for the D-TRONplus and Accu-Chek D-TRONplus insulin pumps from Roche PDF, 29KB, File does not meet accessibility standards Date: 20. June 2006 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 01225/06

Information for the hospital beds Comforta from the company Joh. Stiegelmeyer PDF, 101KB, File does not meet accessibility standards Date: 20. June 2006 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment
Reference 02051/04

Information for the Software RenalSoft Observational Study v.2.0, RenalSoft v.1.1 and Renal Software Suite v.3.1 HD-Modul (Renal Link), Baxter PDF, 4MB, File does not meet accessibility standards Date: 16. June 2006 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 01150/06

Recall of PFO Occluders from AGA Medical PDF, 212KB, File does not meet accessibility standards Date: 16. June 2006 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 01546/06

Corrective action and recall for AutoVue Innova and AutoVue Ultra software version 1.02, Ortho PDF, 52KB, File does not meet accessibility standards Date: 16. June 2006 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01131/06

Recall of Endopath®Probe Plus II Electrosurgical Suction Irrigation Products from Ethicon PDF, 50KB, File does not meet accessibility standards Date: 14. June 2006 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 01162/06

Recall of the Stonetome™ Single-Use Stone Removal Device from Boston Scientific PDF, 357KB, File does not meet accessibility standards Date: 13. June 2006 Topics: Medical devices Type: Customer information

Product group Optics / Precision engineering
Reference 01543/06

Information for the Samaritan Automated External Defibrillator (SAM001, SAM002, SAM003), Heartsine PDF, 512KB, File does not meet accessibility standards Date: 08. June 2006 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 00630/05

Corrections in soft- and hardware of Ipump from Baxter PDF, 43KB, File does not meet accessibility standards Date: 08. June 2006 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 01301/06

Recall of the S4 Adjustable Cross Connector 60-75 MM SW699T from Aesculap PDF, 49KB, File does not meet accessibility standards Date: 07. June 2006 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 01494/06

Recall of the Chiaglia Blue Rhino Percutaneous Tracheostomy Introducer Set from Wiliam Cook PDF, 128KB, File does not meet accessibility standards Date: 06. June 2006 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 01496/06

Recall of the Phadebact CSF Test from Bactus PDF, 211KB, File does not meet accessibility standards Date: 06. June 2006 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 00490/06

Labeling error of the Obtryx™ Transobturator Mid-Urethral Sling System, Boston Scientific PDF, 301KB, File does not meet accessibility standards Date: 06. June 2006 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 01341/06

Recall of NexStent™ Monorail™ Carotid Stent systems, Boston Scientific PDF, 114KB, File does not meet accessibility standards Date: 30. May 2006 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 03390/05

Recall of the Pivot™ Steerable Microcatheters from Boston Scientific PDF, 205KB, File does not meet accessibility standards Date: 30. May 2006 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 01423/06

Corrective action affecting different ICDs from Guidant PDF, 74KB, File does not meet accessibility standards Date: 30. May 2006 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices
Reference 01347/06

Corrective action affecting Ventak Prizm 2 DR. model 1861 manufactured by Guidant Corp. PDF, 139KB, File does not meet accessibility standards Date: 26. May 2006 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices
Reference 02263/04

Corrective action affecting the ICD-models VITALITY HE, RENEWAL 3 and 4 manufactured by Guidant Corp. PDF, 163KB, File does not meet accessibility standards Date: 26. May 2006 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices
Reference 01393/06

Recall of FasT- Fix, Smith & Nephew PDF, 134KB, File does not meet accessibility standards Date: 24. May 2006 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 01143/06

Recall of the artificial saliva solution Salinum, Sinclair Pharma PDF, 62KB, File does not meet accessibility standards Date: 24. May 2006 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 01324/06