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Recall of HI REXPOL Einsatz Dysplasie by Plus Orthopedics PDF, 83KB, File does not meet accessibility standards Date: 03. July 2006 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 01544/06

Corrective action for CRP Latex of Olympus PDF, 43KB, File does not meet accessibility standards Date: 03. July 2006 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01538/06

Recall of Slidex pneumo kit from Biomerieux PDF, 108KB, File does not meet accessibility standards Date: 03. July 2006 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01659/06

Recall of ImmunoCard Toxins A & B, Meridian Bioscience PDF, 290KB, File does not meet accessibility standards Date: 03. July 2006 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01648/06

Corrective action and recall for Cytomics Flow Cytometry Systems, Beckman Coulter PDF, 143KB, File does not meet accessibility standards Date: 03. July 2006 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01600/06

Recall of the Transseptal Sheath, 16.5F with Dilator from ProRhythm PDF, 22KB, File does not meet accessibility standards Date: 03. July 2006 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 01487/06

Information for the stretcher TRIO Mobile Surgery Platform from Stryker PDF, 42KB, File does not meet accessibility standards Date: 30. June 2006 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 01451/06

Recall of Femoral Clamps TKR (slim) by Plus Orthopedics PDF, 118KB, File does not meet accessibility standards Date: 28. June 2006 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 01780/06

Corrective measures of the Gambro Prismaflex™ Continuous Renal Replacement System from Gambro PDF, 78KB, File does not meet accessibility standards Date: 28. June 2006 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 01566/06

Recall of the ambIT Intermittent Ambulatory Infusion Pump from Sorenson PDF, 65KB, File does not meet accessibility standards Date: 28. June 2006 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 01334/06

Information for the Fiamm Sealed Lead Acid Batteries in IVAC® P Series Infusion Pumps from Cardinal Health Alaris® Products PDF, 21KB, File does not meet accessibility standards Date: 27. June 2006 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 01085/06

Recall of the Microcuff Endotracheal Tubes from Unomedical PDF, 886KB, File does not meet accessibility standards Date: 27. June 2006 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 01717/06

Information for the FloSeal-Kits from Baxter PDF, 37KB, File does not meet accessibility standards Date: 27. June 2006 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 01726/06

Recall of MEDAP connection tubes for medical gases, Maquet PDF, 218KB, File does not meet accessibility standards Date: 27. June 2006 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 01355/06

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