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Safety Information for the Versys® and Slotted Provisional Femoral Heads, Zimmer Inc. PDF, 78KB, File does not meet accessibility standards Date: 03. January 2013 Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 07261/12

Lot Recall of STERRAD® NX® System Cassettes REF 10133, ASP PDF, 44KB, File does not meet accessibility standards Date: 03. January 2013 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment - cleaning / disinfection / sterilisation
Reference 07558/12

Lot Recall of the Coaxial Interventional Needles, Innovative Tomography Products GmbH PDF, 444KB, File does not meet accessibility standards Date: 28. December 2012 Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 07673/12

Lot Recall of the Alphacard single-use syringe for intra-atrial ECG lead, B. Braun Melsungen AG PDF, 295KB, File does not meet accessibility standards Date: 28. December 2012 Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 07701/12

Recall of the ENSEAL® G2 Curved and Straight Tissue Sealer devices, Ethicon Endo-Surgery PDF, 33KB, File does not meet accessibility standards Date: 28. December 2012 Type: Customer information

Product group Electromedical fields
Reference 07325/12

Recall for Antimicrobial Susceptibility Testing Disc, Oxoid PDF, 17KB, File does not meet accessibility standards Date: 27. December 2012 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - microbiological products
Reference 07555/12

Lot Recall of TRIGEN INTERTAN nails, SMITH & NEPHEW PDF, 97KB, File does not meet accessibility standards Date: 27. December 2012 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 07646/12

Safety Notice concerning the Metran High Frequency Oscillation Ventilator model R100/Vision a, Novalung PDF, 453KB, File does not meet accessibility standards Date: 27. December 2012 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - anaesthesia and medical gas supply
Reference 07357/12

Safety Notice concerning LIVOPAN systems, Linde Gas Therapeutics PDF, 98KB, File does not meet accessibility standards Date: 27. December 2012 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - anaesthesia and medical gas supply
Reference 07611/12

Recall of the ARDIS Inserter worldwide, Zimmer Inc. PDF, 131KB, File does not meet accessibility standards Date: 27. December 2012 Type: Customer information

Product group Medical instruments for use in humans
Reference 07561/12

Recall of GlideScope GVL video laryngoscope, Verathon PDF, 2MB, File does not meet accessibility standards Date: 20. December 2012 Topics: Medical devices Type: Customer information

Product group Optics / Precision engineering - medical microscopes (does not incude laboratory microscopes)
Reference 06957/12

Corrective Action concerning Oxoid Columbia Agar with Sheep Blood PLUS PB 5039 A (Lot- No: 1262841) due to a microbial contamination, OXOID PDF, 108KB, File does not meet accessibility standards Date: 17. December 2012 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - microbiological products
Reference 07105/12

Field Safety Notice concerning a corrective action of Corpuls 3 defibrillators to which software versions 2.0.0 and 2.0.2 have been installed, GS Elektromedizinische Geräte G. Stemple GmbH PDF, 503KB, File does not meet accessibility standards Date: 17. December 2012 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrotherapy
Reference 07316/12

Lot Recall for Perthese & Perthese Esthea Breast Implants, Perouse Plastie PDF, 92KB, File does not meet accessibility standards Date: 12. December 2012 Topics: Medical devices Type: Customer information

Product group Non-active implants - special implants
Reference 07319/12

Recall for several RUMI ARCH® and Advincula Arch™ uterine manipulation handles, Cooper Surgical PDF, 56KB, File does not meet accessibility standards Date: 12. December 2012 Type: Customer information

Product group Medical instruments for use in humans
Reference 07453/12

Recall for Wang Transbronchial Aspiration Needles, ConMed Corporation PDF, 56KB, File does not meet accessibility standards Date: 12. December 2012 Type: Customer information

Product group Medical instruments for use in humans
Reference 07367/12

Recall flexible drills, tantum PDF, 37KB, File does not meet accessibility standards Date: 07. December 2012 Type: Customer information

Product group Medical instruments for use in humans
Reference 07007/12

Refitting of wheelchairs LifeStand LSCO, Permobil PDF, 135KB, File does not meet accessibility standards Date: 07. December 2012 Topics: Medical devices Type: Customer information

Product group Orthopaedic / Rehabilitation technology - mobility aids
Reference 07303/12

Field Safety Notice concerning potentially falsely placed electronic left/right markers on DigitalDiagnost X-ray systems, Philips Medical Systems PDF, 94KB, File does not meet accessibility standards Date: 06. December 2012 Topics: Medical devices Type: Customer information

Product group Radiological technology - stationary radiological equipment
Reference 07296/12