BfArM - Federal Institute for Drugs and Medical Devices

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Becton Dickinson recalls several lot numbers of the peridural anaesthesia products PDF, 147KB, File does not meet accessibility standards Date: 29. December 2005 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 03139/05

Corrective action and recall of Dade Behring for the BEP 2000 and the BEP 2000 Advance System PDF, 76KB, Date: 29. December 2005 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03099/05

Baxter recalls the Intercept BC Platelet Pooling Set and Buffy Coat Pooling Set PDF, 136KB, Date: 29. December 2005 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 03042/05

Safety risk with the BINGO mobility base from Hoggi PDF, 28KB, Date: 22. December 2005 Topics: Medical devices Type: Customer information

Product group Orthopaedic / Rehabilitation technology
Reference 03002/05

Potential therapy failure of Sigma pacemakers from Medtronic PDF, 23KB, Date: 22. December 2005 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices
Reference 02984/05

OrbusNeich recalls the SafeCut Coronary Dilatation Catheter PDF, 237KB, Date: 22. December 2005 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 02979/05

Corrective action and recall of Ortho Clinical Diagnostics for AutoVue Innova/Ultra PDF, 55KB, Date: 22. December 2005 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03110/05

Recall of Becton Dickinson for the BD™ PhoenixSpec™ Calibrator Kit PDF, 95KB, Date: 22. December 2005 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03239/05

Maquet recalls the surgical suction unit Medap Twista SP 1070 PDF, 670KB, Date: 21. December 2005 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 02699/05

MEDRAD recalls the heat maintainers used on the MEDRAD Stellant CT Injector System PDF, 248KB, Date: 21. December 2005 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 02761/05

Exchange of the Gold Hub Capistrano-, Gold Hub Finesse- and Gold Hub Monty Cannula from HK Surgical PDF, 116KB, Date: 21. December 2005 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 02438/05

Corrective action and recall of Becton Dickinson for the BBL™ GasPak™ Anaerob Pouch System and Campy Pouch System PDF, 74KB, Date: 21. December 2005 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03200/05

Stryker recalls the StrykeFlow 2 pump and Handpiece with 10 feet of Tubing PDF, 149KB, Date: 21. December 2005 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 02969/05

Recall of tangoRS-spinal instrumentation systems from Ulrich PDF, 77KB, Date: 12. December 2005 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 02896/05

ConMed Linvatec recalls the MicroChoice ® Footswitch and ConMed Linvatec 3 Pedal Footswitch PDF, 98KB, Date: 12. December 2005 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 02308/05

Recall of DPC Biermann Immulite 2000 and 2500 Cortisol and Immulite 2000 Folic acid PDF, 52KB, Date: 12. December 2005 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02917/05

Recall of Dade Behring for the Dimension clinical chemistry system RCRP PDF, 43KB, Date: 12. December 2005 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03128/05

Merit Medical recalls the IntelliSystem II Thermal Dot Matrix Printer IN1600/IN1650 PDF, 89KB, Date: 08. December 2005 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 02821/05

Encore Medical recalls Foundation and 3DKnee Non-Porous Baseplates PDF, 37KB, Date: 08. December 2005 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 02885/05

Smith & Nephew recall the sterile wound dressing Opsite Post-Op PDF, 88KB, Date: 08. December 2005 Topics: Medical devices Type: Customer information

Product group Dressings / Pads
Reference 02808/05

Recall of Dade Behring for N Latex SAA OQMP PDF, 60KB, Date: 08. December 2005 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02895/05

Corrective action of Dade Behring for Complement Reagents PDF, 61KB, Date: 08. December 2005 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02869/05

DePuy Orthopaedics recalls the Acclaim Total Elbow Joint Replacement Implant PDF, 112KB, Date: 05. December 2005 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 02985/05

Corrective action on Sola 300 from Dräger PDF, 54KB, File does not meet accessibility standards Date: 05. December 2005 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 02061/05

Otto Bock recalled the powered wheelchairs C1000 and B600 PDF, 84KB, Date: 02. December 2005 Topics: Medical devices Type: Customer information

Product group Orthopaedic / Rehabilitation technology
Reference 02983/05

Recall of Hedstrom Files from Kerr Hawe PDF, 95KB, Date: 02. December 2005 Topics: Medical devices Type: Customer information

Product group Dental products
Reference 02868/05

Boston Scientific recalls the MAVERIK™ Monorail™ catheter PDF, 99KB, Date: 02. December 2005 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 02946/05

Corrective action of BioMerieux for ID 32, Rapid ID 32, Rapid ATB and ATB identification strips PDF, 130KB, Date: 02. December 2005 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03021/05

Corrective action of Roche for COBAS Ampliprep/COBAS TaqMan tests PDF, 308KB, Date: 02. December 2005 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02253/05

Cardiac Science recalls the Powerheard AED G3s PDF, 96KB, Date: 02. December 2005 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 01354/05