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
Director, Litigation & Investigations EMEA
Gilead Sciences
Stockely Park
Assistant General Counsel/Senior Corporate Counsel
Genentech
South San Francisco, CA
Senior Analyst Compliance
Edwards Lifesciences
Irvine, CA
Legal Counsel
Alcon
Fort Worth, TX
Director, Senior Legal Counsel
Alcon
Fort Worth, TX