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.

View Full Article in:

MassDevice.com (Boston)

Published in Brief:

SmartBrief Job Listings for Health Care

Job Title Company Location
Neurovascular Intervention Product Sales Rep, North East
ASAHI INTECC
Multiple Locations, SL_Multiple Locations
Senior Manager, Compliance
Stryker
Fremont, CA
Director, Office of Device Evaluation
FDA, Center for Devices and Radiological Health
Silver Spring, MD
Director, Office of Compliance
FDA, Center for Devices and Radiological Health
Silver Spring, MD
Food & Drug Associate
Confidential
Washington, D.C., DC