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Recalls of Cardiac Implants in the Last Decade: What Lessons Can We Learn? PLOS ONE, May 2015 Shixuan Zhang, Christine Kriza, Sandra.Manufacturer’s Field Safety Corrective Action Report. (MHRA) Devices – UK. Once Recall Acknowledgement and Return Form received by Integra and if they have.

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The MHRA has issued one recall since June 2007 for one batch of falsified product prescribed for the treatment of chronic asthma. This product was intercepted at a.

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Reporting of Adverse Events for NUH sponsored Medical Device Trials Page 1 Effective date 12/09/12 CONTENTS SECTION TITLE PAGE 1 Introduction 3.

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