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Recall and corrective action for Coulter LH 500 Hematology Analyzer PN 178832, 178833 und 178834, Beckman Coulter PDF, 121KB, File does not meet accessibility standards Date: 10. May 2006 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01271/06

Smith & Nephew recalls the Knee-System Genesis II PDF, 40KB, File does not meet accessibility standards Date: 09. May 2006 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 01246/06

Advice for the Olympus LUS/LUS-2 Ultrasonic Lithotriptor PDF, 45KB, File does not meet accessibility standards Date: 09. May 2006 Topics: Medical devices Type: Customer information

Product group Ultrasonics
Reference 00660/06

Label error of Achalasia Balloon Dilators by Boston Scientific PDF, 293KB, File does not meet accessibility standards Date: 05. May 2006 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 01197/06

Recall of tubes for liposuction by Microaire® Surgical Instruments PDF, 53KB, File does not meet accessibility standards Date: 05. May 2006 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 01160/06

Corrective action for Access Immunoassay Systems CEA, Beckman Coulter PDF, 65KB, File does not meet accessibility standards Date: 05. May 2006 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01221/06

Recall and corrective action for OneTouch® GlucoTouch® blood glucose analyzers, Lifescan PDF, 518KB, File does not meet accessibility standards Date: 05. May 2006 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 00829/06

Corrective action of Dade Behring for Stratus® CS Analyzer PDF, 252KB, File does not meet accessibility standards Date: 05. May 2006 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01048/06

Gerätebau Felix Schulte recalls Iris lamps Planilux Date: 04. May 2006 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 00881/06

Correction of LIFEPAK® 12 und LIFEPAK® 20, Medtronic PDF, 34KB, File does not meet accessibility standards Date: 03. May 2006 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 00900/06

Recall of DAKO Envision™+, Dako Cytomation PDF, 27KB, File does not meet accessibility standards Date: 03. May 2006 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01202/06

Corrective action and recall for Glucose HK MOD P/D R2, Roche PDF, 58KB, File does not meet accessibility standards Date: 03. May 2006 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 00968/06

Correction of the temporomandibular joint program TM 4, SIRONA PDF, 15KB, File does not meet accessibility standards Date: 03. May 2006 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 01087/06

Recall of Ball tip guide rods of the TriGen nail system, Smith & Nephew PDF, 52KB, File does not meet accessibility standards Date: 03. May 2006 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 00738/06

Software update for Precision 500D X-ray systems, GE Healthcare PDF, 56KB, File does not meet accessibility standards Date: 28. April 2006 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 00965/06

BioMerieux recalls the Slidex Rota-Kit 2 PDF, 94KB, File does not meet accessibility standards Date: 28. April 2006 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01149/06

Delphi recalls the IVantage® Infusion System PDF, 35KB, File does not meet accessibility standards Date: 28. April 2006 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 01071/06

Corrective action for scooters Maxi 4 and Midi 4 plus, Days Healthcare PDF, 54KB, File does not meet accessibility standards Date: 28. April 2006 Topics: Medical devices Type: Customer information

Product group Orthopaedic / Rehabilitation technology
Reference 01108/06

Recall of Acon Laboratories for the Quick-Chek Drug Screen PDF, 57KB, File does not meet accessibility standards Date: 27. April 2006 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 00699/06

Smith Medical recalls the Portex Spinal Epidural Needle Sets PDF, 268KB, File does not meet accessibility standards Date: 27. April 2006 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 01067/06

Information for the Harrison Fetal Bladder Stent Sets from COOK PDF, 75KB, File does not meet accessibility standards Date: 27. April 2006 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 00788/06

Replacement kits for wheelchairs Rea 705 Silencio-Care, Invacare PDF, 35KB, File does not meet accessibility standards Date: 27. April 2006 Topics: Medical devices Type: Customer information

Product group Orthopaedic / Rehabilitation technology
Reference 00848/06

St Jude Medical recalls Agilis Steerable Introducers PDF, 220KB, File does not meet accessibility standards Date: 27. April 2006 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 01079/06

Corrective action and recall for Ortho AutoVue and AutoVue Ultra PDF, 199KB, File does not meet accessibility standards Date: 27. April 2006 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 00841/06

Gambro recalls the dialysis blood tubing system Prisma and HF PDF, 358KB, File does not meet accessibility standards Date: 27. April 2006 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 02837/05

Össur recalls the prosthetic knees Total Knee PDF, 20KB, File does not meet accessibility standards Date: 27. April 2006 Topics: Medical devices Type: Customer information

Product group Orthopaedic / Rehabilitation technology
Reference 00945/06

Tyco Healthcare recalls percutaneous tracheostomy tubes PDF, 71KB, File does not meet accessibility standards Date: 26. April 2006 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 02283/05

Information about the Transseptal Sheath from the company ProRhythm PDF, 43KB, File does not meet accessibility standards Date: 25. April 2006 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 00471/06

Recall of the product Tiger Tube Self-Advancing Nasal Jejunal Feeding Tube from the manujfacturer William Cook Europe PDF, 78KB, File does not meet accessibility standards Date: 25. April 2006 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 00481/06

Corrective action of x-ray systems from Philips PDF, 83KB, File does not meet accessibility standards Date: 25. April 2006 Topics: Medical devices Type: Customer information

Product group Ultrasonics
Reference 00984/06