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Biotronik carpeted by FDA over ICD (implantable cardioverter defibrillator) recall faults

This article was originally published in Clinica

Executive Summary

The US FDA has issued a warning letter to the German manufacturer Biotronik for failing to inform the agency about a recall regarding the company's Belos VR and Belos VR-T implantable cardioverter defibrillators (ICDs).

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