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Archive - Nov 12, 2009

Date

Synthes USA, Ti Synex II Vertebral Body Replacement - Class I Recall

Reports of loss of device height, which may result in nerve injury, increased pain, spinal compression fracture, failure of additional fixation, and/or need for surgery to modify the implanted device.

Disaster Preparedness in Pediatric Type 1 Diabetes Mellitus

The objective of this study is to assess emergency...

Meeting the health needs of children and young people: a...

This guidance calls on NHS trusts to adapt to changing...