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Lot Recall of the CHEX Circular Stapler, Frankenman International Limited PDF, 113KB, File does not meet accessibility standards Date: 22. July 2013 Type: Customer information

Product group Medical instruments for use in humans - general instruments
Reference 02875/13

Corrective action for Dimension Vista 500® and Dimension® Vista 1500, Siemens PDF, 30KB, File does not meet accessibility standards Date: 18. July 2013 Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 03107/13

Corrective action for FSH One Step Menopause Test Device (Urine), Innovacon PDF, 416KB, File does not meet accessibility standards Date: 18. July 2013 Type: Customer information

Product group In-vitro diagnostics - immunological products
Reference 03729/13

Recall of the GENESIS II Cruciate Retaining Insert Trials, Smith & Nephew PDF, 53KB, File does not meet accessibility standards Date: 18. July 2013 Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 03877/13

Corrective action for IH-1000, Bio-Rad Laboratories PDF, 914KB, File does not meet accessibility standards Date: 18. July 2013 Type: Customer information

Product group In-vitro diagnostics - haematological, histological and cytological products
Reference 02866/13

Lot Recall of the 27 G disposable cannula provided with the Amvisc® und Amvisc® Plus viscoelastic devices, Bausch & Lomb PDF, 2MB, File does not meet accessibility standards Date: 18. July 2013 Topics: Medical devices Type: Customer information

Product group ophthalmological technology - liquid media for ophthalmological purposes
Reference 07483/12

Corrective action for the Multidrogen Speicheltest, Ökonomed PDF, 32KB, File does not meet accessibility standards Date: 18. July 2013 Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 03829/13

Recall of Hand pendants for OPERON D 850, D 820 und D 760 operating tables, Berchtold PDF, 75KB, File does not meet accessibility standards Date: 18. July 2013 Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 01227/13

Lot Recall for BioMend®, BioMend Extend™, CollaCote®, CollaPlug® and CollaTape®, INTEGRA PDF, 54KB, File does not meet accessibility standards Date: 18. July 2013 Topics: Medical devices Type: Customer information

Product group Dental products - others
Reference 03167/13

Safety Notice for the High Energy Clinacs®, Varian Medical Systems PDF, 92KB, File does not meet accessibility standards Date: 17. July 2013 Type: Customer information

Product group Radiotherapy / Radiation protection - radiation facilites with accelerators for teletherapy
Reference 03220/13