WebApr 9, 2010 · for Recall: Hospira has received numerous customer complaints of the Symbiq infusion pump's failure to detect air-in-line conditions during operation. FDA Determined Cause 2: Device Design: Action:... WebAug 3, 2015 · Hospira Inc. stopped making Symbiq pumps in 2013 and said it expected most of them would be replaced within two to three years. The Lake Forest, Illinois, …
Citing hacking risk, FDA says Hospira pump shouldn
WebAug 29, 2012 · We recently wrote that Hospira, Inc. announced a recall of its Hydromorphone Injection due to overdose concerns. That recall involved one lot of Hydromorphone Injection and followed a reported complaint of a single Carpuject containing more than the 1 mL labeled fill volume. WebMar 8, 2012 · The Symbiq device's FDA clearance is not expected to impact Hospira's 2012 financial projections, which were issued on Feb. 14, 2012. About Hospira Hospira, Inc. is the world's leading provider of ... is farmfoods closing down
Hospira gets warning letter after FDA inspection - Yahoo News
WebAug 5, 2015 · The FDA issued an advisory on Friday about the Hospira Symbiq Infusion System v3.13 and earlier, following a Department of Homeland Security ICS-CERT warning on the system back in June. It explained: “Hospira and an independent researcher confirmed that Hospira’s Symbiq Infusion System could be accessed remotely through a hospital’s … WebJul 31, 2015 · 31 July 2015, 5:50 pm By Jim Finkle BOSTON (Reuters) - The U.S. Food and Drug Administration on Friday advised hospitals not to use Hospira Inc's Symbiq infusion system, saying a security... WebMar 11, 2012 · Hospira, a provider of injectable drugs and infusion technologies, has gained regulatory clearance from the US Food and Drug Administration (FDA) for its Symbiq 3.13 infusion device, the improved version of the company’s infusion system platform. The Symbiq infusion system is a device designed to help improve workflow and decrease … is farmers owned by zurich