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14,950 results

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Kerr recalls the adhesive system Optibond Solo Plus PDF, 144KB, File does not meet accessibility standards Date: 06. April 2006 Topics: Medical devices Type: Customer information

Product group Dental products
Reference 00651/06

CMA/Microdialysis recalls the CMA 61 Hepatic Microdialysis Catheters PDF, 50KB, File does not meet accessibility standards Date: 06. April 2006 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 00885/06

Biotest recalls the tranfusion device TMSB-3 PDF, 41KB, File does not meet accessibility standards Date: 06. April 2006 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 00633/06

Upgrade Kits of Hemodiaysis Instruments from Baxter PDF, 169KB, File does not meet accessibility standards Date: 06. April 2006 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 00696/06

Recall of transducers 8667 from B-K Medical PDF, 37KB, File does not meet accessibility standards Date: 05. April 2006 Topics: Medical devices Type: Customer information

Product group Ultrasonics
Reference 00758/06

Corrective action and recall Synchromn LX20 and Synchron LX20 Pro Clinical Systems, Beckman Coulter PDF, 149KB, File does not meet accessibility standards Date: 05. April 2006 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 00879/06

B.Braun/Aesculap recalls Endoscopy Trolleys PDF, 45KB, File does not meet accessibility standards Date: 31. March 2006 Topics: Medical devices Type: Customer information

Product group Optics / Precision engineering
Reference 02252/05

Recall of Proceed Surgical Mesh from Ethicon PDF, 165KB, File does not meet accessibility standards Date: 30. March 2006 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 00015/06

Corrective action of the computed tomography systems Brilliance from Philips PDF, 310KB, File does not meet accessibility standards Date: 30. March 2006 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 00818/06

Corrective action from Olympus for Glucose OSR 6X21 and Glucose STAT OSR6140 PDF, 47KB, File does not meet accessibility standards Date: 30. March 2006 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 00828/06

WaveLight recalls the acrylic intraocular lenses Acriflex 47CSE and 48CSE Date: 28. March 2006 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 00465/06

Ev3 recalls the XSizer® Thrombectomy-Catheter System PDF, 79KB, File does not meet accessibility standards Date: 28. March 2006 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 00592/06

Carl Zeiss Meditec recalls the MEL 80 with CRS-Master and WASCA ANALYZER PDF, 154KB, File does not meet accessibility standards Date: 28. March 2006 Topics: Medical devices Type: Customer information

Product group ophthalmological technology
Reference 00640/06

Missing directions for use at the Embolic Protection Systems and the Retrieval Sheaths from Boston Scientific PDF, 48KB, File does not meet accessibility standards Date: 28. March 2006 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 00765/06

Recall of Biomerieux for Slidex Strepto-Kit, Slidex Strepto B and Slidex Strepto D PDF, 175KB, File does not meet accessibility standards Date: 28. March 2006 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 00819/06

Advanced Bionics recalls the Implantable Cochlear Stimulators PDF, 114KB, File does not meet accessibility standards Date: 28. March 2006 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices
Reference 00724/06

Low level current in CONTAK RENEWAL 3 RF and CONTAK RENEWAL 4 RF from Guidant PDF, 37KB, File does not meet accessibility standards Date: 28. March 2006 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices
Reference 00679/06

Fisher & Paykel recalls the dual heated breathing circuits PDF, 211KB, File does not meet accessibility standards Date: 28. March 2006 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 03371/05

Information on Scooter Sungift 500 Date: 28. March 2006 Topics: Medical devices Type: Article

Scooter Sungift 500 manufactured by Sungift PLC (Great Britain) has been withdrawn from the Norwegian market in 2005

Unomedical recalls the Microcuff Pediatric Endotracheal Tubes PDF, 58KB, File does not meet accessibility standards Date: 24. March 2006 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 00759/06

Remedy possibilities in case of leakages of the RetrO and XpressO dialysis catheters from Spire Biomedical PDF, 47KB, File does not meet accessibility standards Date: 24. March 2006 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 00547/06

Recall of Bipolar Forceps from Tyco Healthcare PDF, 63KB, File does not meet accessibility standards Date: 24. March 2006 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 00245/06

Recall of Bipolar Forceps from ERBE Elektromedizin PDF, 109KB, File does not meet accessibility standards Date: 24. March 2006 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 00245/06

Field corrective action regarding the MIS Anterolateral Instrument Sets from Zimmer PDF, 439KB, File does not meet accessibility standards Date: 24. March 2006 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 00411/06

Problems with some LCD displays of the Cell Saver 5, Cell Saver 5+, and MCS+ 9000 from Haemonetics PDF, 114KB, File does not meet accessibility standards Date: 24. March 2006 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 00578/06

TRUMPF recalls the Head Rest for Shoulder Operation PDF, 42KB, File does not meet accessibility standards Date: 24. March 2006 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 00349/06

Medsorb Dominicana recalls the Ivalon Nasal Sponge PDF, 58KB, File does not meet accessibility standards Date: 24. March 2006 Topics: Medical devices Type: Customer information

Product group Dressings / Pads
Reference 00650/06

Corrective action of Tosoh Bioscience for HbA1c-Control PDF, 46KB, File does not meet accessibility standards Date: 24. March 2006 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 00500/06

Corrective action of Bayer for Advia 1200, Advia 1650 and Advia 2400 Systems PDF, 156KB, File does not meet accessibility standards Date: 24. March 2006 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 00609/06

Recall of Niti-S Colorectal-Stents from Taewoong Medical PDF, 58KB, File does not meet accessibility standards Date: 24. March 2006 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 00550/06