FDA Recalls List – October 22, 2014
This article was originally published in The Gray Sheet
Executive Summary
The agency's Oct. 22 enforcement report includes six class I recall actions from Covidien tied to findings that its defibrillation electrodes are not compatible with certain Philips' automated external defibrillators. In total, the report lists 22 recalls, including 15 class IIs and one class III action.