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14,972 results

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Recall for the Coroflex Isar Coronary stent, B. Braun Melsungen AG, Division Aesculap Vascular Systems PDF, 2MB, File does not meet accessibility standards Date: 03. June 2015 Topics: Medical devices Type: Customer information

Product group Non-active implants - special implants
Reference 03447/15

Corrective action for Artis zee Floor, Artis zee Biplane, Artis zee Multi Purpose systems, Siemens Healthcare PDF, 386KB, File does not meet accessibility standards Date: 03. June 2015 Topics: Medical devices Type: Customer information

Product group Radiological technology - radiological equipment for vascular diagnostics
Reference 03280/15

Corrective action for Alcon Monarch® IOL Delivery System Cartridges, Alcon Laboratories Inc./Alcon Pharma GmbH PDF, 208KB, File does not meet accessibility standards Date: 03. June 2015 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - eye surgery
Reference 03289/15

Urgent Safety Notice for the Hospira GemStar Family of infusers, Hospira Inc. PDF, 294KB, File does not meet accessibility standards Date: 03. June 2015 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - infusion technology
Reference 03041/15

Recall for the Covidien Devon Light Gloves (Light handle covers), ArcRoyal Ltd. PDF, 2MB, File does not meet accessibility standards Date: 03. June 2015 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 03272/15

Urgent Safety Notice for the Crystalens® AO Intra Ocular Lenses, Bausch + Lomb Surgical Division PDF, 160KB, File does not meet accessibility standards Date: 02. June 2015 Topics: Medical devices Type: Customer information

Product group Non-active implants - special implants
Reference 00376/15

Recall for the Steel cannula infusion sets, Unomedical a/s PDF, 135KB, File does not meet accessibility standards Date: 02. June 2015 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - infusion technology
Reference 03274/15

Corrective action for the Pulsar-18 and Pulsar-35 peripheral self-expanding Nitinol stent systems, Biotronik AG PDF, 83KB, File does not meet accessibility standards Date: 02. June 2015 Topics: Medical devices Type: Customer information

Product group Non-active implants - special implants
Reference 03047/15

Recall of the 4.5 mm Cortical Screws listed as compatible with the M/DN system, Zimmer Inc. PDF, 67KB, File does not meet accessibility standards Date: 02. June 2015 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 03200/15

Recall for the product Gelseal Straight, Vascutek Ltd. PDF, 139KB, File does not meet accessibility standards Date: 02. June 2015 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 03198/15

Increased risk of cardiovascular death with use of ASV therapy (Weinmann devices SOMNOvent CR and prismaCR), Weinmann Geräte für Medizin GmbH + Co. KG PDF, 210KB, File does not meet accessibility standards Date: 02. June 2015 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - anaesthesia and medical gas supply
Reference 03027/15

Corrective action for the MAGNUS Hybrid OR table, MAQUET GmbH PDF, 796KB, File does not meet accessibility standards Date: 01. June 2015 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 03215/15

Recall for the product TRACOE vario Tracheostomy Tube, TRACOE medical GmbH PDF, 295KB, File does not meet accessibility standards Date: 01. June 2015 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - anaesthesia and medical gas supply
Reference 02982/15

Corrective action for the Spectron Multi Med Light valves, Spectron Gas Control Systems GmbH PDF, 100KB, File does not meet accessibility standards Date: 01. June 2015 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - anaesthesia and medical gas supply
Reference 01979/15

Safety Notice concerning CombiSets® containing Medtronic Covidien Devon™ Light Glove, Paul Hartmann AG PDF, 41KB, File does not meet accessibility standards Date: 01. June 2015 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 02871/15

Urgent Safety Notice for the IntraClude™ intra-aortic occlusion device Model ICF100, Edwards Lifesciences PDF, 48KB, File does not meet accessibility standards Date: 01. June 2015 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 03138/15

Urgent Safety Notice for the DuraDiagnost 3.0/4.0 X-Ray System, Philips Healthcare (Suzhou) Co. Ltd. PDF, 119KB, File does not meet accessibility standards Date: 01. June 2015 Topics: Medical devices Type: Customer information

Product group Radiological technology - stationary radiological equipment
Reference 03045/15

Urgent Field Safety Notice, IMC-15-11.A.OUS, IMMULITE® 2000, IMMULITE® 2000 XPi
Italian Cypress Allergen Shelf-Life Stability, Siemens
PDF, 47KB, File does not meet accessibility standards
Date: 28. May 2015 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - immunological products
Reference 02996/15

Recall of recomScan Version 3.4, Build-Versionen below 62, MIKROGEN GmbH PDF, 100KB, File does not meet accessibility standards Date: 28. May 2015 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - microbiological products
Reference 03022/15

The influence of low-molecular-weight heparin (LMWH)
on DNA in the blood plasma of pregnant women, LifeCodexx AG,
Date: 28. May 2015 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - others
Reference 03054/15

URGENT - Field Safety Notice
Philips Model AFFINITI 70 Ultrasound System, Philips
PDF, 216KB, File does not meet accessibility standards
Date: 28. May 2015 Topics: Medical devices Type: Customer information

Product group Ultrasonics - ultrasonic diagnostic equipment
Reference 03031/15

URGENT - Field Safety Notice
Philips Model EPIQ 5 Ultrasound System, Philips
PDF, 210KB, File does not meet accessibility standards
Date: 28. May 2015 Topics: Medical devices Type: Customer information

Product group Ultrasonics - ultrasonic diagnostic equipment
Reference 03032/15

URGENT – Field Safety Notice for Philips IntelliVue Information Center (PIIC) iX, Philips PDF, 380KB, File does not meet accessibility standards Date: 28. May 2015 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrodiagnostics
Reference 03111/15, 03052/15

Corrective action for the Philips Ultrasound AFFINITI 50 Ultrasound System, Philips Healthcare Ultrasound PDF, 224KB, File does not meet accessibility standards Date: 21. May 2015 Topics: Medical devices Type: Customer information

Product group Ultrasonics - ultrasonic diagnostic equipment
Reference 03034/15

Corrective action for the Philips Model EPIQ 7 Ultrasound System, Philips Healthcare Ultrasound PDF, 222KB, File does not meet accessibility standards Date: 21. May 2015 Topics: Medical devices Type: Customer information

Product group Ultrasonics - ultrasonic diagnostic equipment
Reference 03033/15

Urgent Safety Notice for the product Remel PathoDx Strep B Group Latex, Remel Inc. (Part of Thermo Fisher Scientific) PDF, 71KB, File does not meet accessibility standards Date: 21. May 2015 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - microbiological products
Reference 02934/15

Urgent Safety Notice for the products AllSet+ Gold and UniTray, Life Technologies PDF, 279KB, File does not meet accessibility standards Date: 21. May 2015 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - instruments, apparatuses and systems
Reference 02784/15

Further Information/Corrective action for specific Neuromuscular Transmission Modules (E-NMT-00 and M-NMT-02), GE Healthcare PDF, 107KB, File does not meet accessibility standards Date: 21. May 2015 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrodiagnostics
Reference 03647/14