H&H Medical's device recall labeled as Class I by FDA

10/25/2013 | MassDevice.com (Boston)

H&H Medical has recalled some of its emergency cricothyrotomy kits, intended for use by first-responder trauma and battlefield experts, over concerns that the endotracheal tube cuff balloon used with the devices may not function properly. The recall, which covers kits produced from Aug. 7, 2012, to July 29, 2013, has been categorized as Class I by the FDA.

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MassDevice.com (Boston)

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