Synthes issues recall over spinal implants
Synthes voluntarily recalled Synex II Central Body components after it received six reports of adverse events, a move classified by the FDA as a Class I recall. The company has told surgeons and hospitals to stop using the spinal implants immediately.
Philadelphia Inquirer, The | 11/04
This story published in AdvaMed SmartBrief on 11/05/2009
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