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Batch recall of Cellfina System Prep Pack CP1, Merz Pharmaceuticals GmbH PDF, 68KB, File does not meet accessibility standards Date: 28. November 2016 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 10004/16

Urgent field safety notice for Avance CS2 / Avance / Amingo, GE Healthcare PDF, 143KB, File does not meet accessibility standards Date: 28. November 2016 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - anaesthesia and medical gas supply
Reference 10189/16

Urgent field safety notice for fabian HFO / evolution, ACUTRONIC Medical Systems AG PDF, 76KB, File does not meet accessibility standards Date: 28. November 2016 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - anaesthesia and medical gas supply
Reference 09824/16

Urgent field safety notice for Mobile Digital X-Ray GM60A, Samsung Electronics PDF, 40KB, File does not meet accessibility standards Date: 28. November 2016 Topics: Medical devices Type: Customer information

Product group Radiological technology - mobile radiological diagnostic facilities
Reference 09815/16

Lot recall of Drill 1 and 2 / Twist Drill PRO / Starter Set, Straumann GmbH PDF, 51KB, File does not meet accessibility standards Date: 28. November 2016 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 10214/16

Batch recall of D-Dimer Rapid Test D-DIMK20, Diagnostik Nord GmbH PDF, 225KB, File does not meet accessibility standards Date: 28. November 2016 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - haematological, histological and cytological products
Reference 03622/16

Urgent Field Safey Notice for RayStation 4.0 / 4.5 / 4.7 and 5.0, RaySearch Laboratories PDF, 307KB, File does not meet accessibility standards Date: 24. November 2016 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection - radiotherapy treatment planning systems
Reference 09621/16

Recall of Acuvance®2 Safety Catheter, Smiths Medical ASD PDF, 214KB, File does not meet accessibility standards Date: 23. November 2016 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - syringes and cannulas
Reference 10081/16

Lot recall of WECK Visistat 35W, Teleflex Medical PDF, 183KB, File does not meet accessibility standards Date: 23. November 2016 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - general instruments
Reference 10088/16

Recall of CELON ELITE ESG-200 / Model Number WA90001A, OLYMPUS Deutschland GmbH PDF, 183KB, File does not meet accessibility standards Date: 23. November 2016 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrotherapy
Reference 10049/16

Lot recall of GREATBATCH Medical Offset Reamer Handle (00-7804-080-00), Zimmer Biomet PDF, 430KB, File does not meet accessibility standards Date: 23. November 2016 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 10082/16

Lot / batch recall of Bridge Occlusion Ballon, Spectranetics Corporation PDF, 100KB, File does not meet accessibility standards Date: 22. November 2016 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 09763/16

Lot / batch recall of Turbo Elite atherectomy catheter / ELCA coronary atherectomy catheter, Spectranetics Corporation PDF, 68KB, File does not meet accessibility standards Date: 22. November 2016 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 09761/16, 09766/16

Recall of SONNET Mini Battery Pack Cable, MED-EL Elektromedizinische Geräte GmbH PDF, 148KB, File does not meet accessibility standards Date: 22. November 2016 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices - biostimulators
Reference 09211/16

Lot recall of ART-1023 Quinn’s Advantage Medium with Hepes, CooperSurgical Inc. / ORIGIO PDF, 195KB, File does not meet accessibility standards Date: 21. November 2016 Topics: Medical devices Type: Customer information

Product group Physical therapy - others
Reference 09966/16

Batch recall of Reflection Dead Blow Mallet, Smith & Nephew Inc. PDF, 82KB, File does not meet accessibility standards Date: 21. November 2016 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 09953/16

Urgent field safety notice for Elekta AB / IMPAC Medical Systems Inc. PDF, 119KB, File does not meet accessibility standards Date: 18. November 2016 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection - radiotherapy treatment planning systems
Reference 09685/16

Urgent field safety notice for IMMULITE 2000 / XPi, Siemens Healthcare Diagnostics Inc. PDF, 27KB, File does not meet accessibility standards Date: 18. November 2016 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 09784/16

Urgent field safety notice for Double Balloon Catheter / Isofuse Isolation Aspiration Catheter, Delcath Systems Inc. PDF, 326KB, File does not meet accessibility standards Date: 18. November 2016 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - therapeutic apheresis procedures
Reference 04157/16

Lot recall of E.MOTION PS PRO MENISCAL COMPONENT F3L 20 mm, Aesculap AG PDF, 498KB, File does not meet accessibility standards Date: 17. November 2016 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 09187/16