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for Recall: Animas determined that keypad wear over time was contributing to an increased complaint rate associated with damaged keypads on the Vibe Insulin Infusion Pump and System....
Animas Corporation sent an "Urgent: Insulin Pump Recall" letter dated July, 29 20011 to all affected customers. The letter included affected product and problem. They requested anyone who...
Recall of Animas Vibe Insulin Infusion Pump and System. According to U.S. Food and Drug Administration, this recall involved a device in United States that was produced by Animas Corporation . A correction or removal action taken by a manufacturer to address a problem with a medical device.
Explore more than 120,000 Recalls, Safety Alerts and Field Safety Notices of medical devices and their connections with their manufacturers.
9 kwi 2013 · The FDA has issued a Class I recall notice relating to the Animas® 2020 Insulin Pump. It seems there are two problems with the device. A Class I recall notice, is the FDA's most serious type of recall and reserved for cases where human health is at risk by continued use of the device.
24 mar 2017 · Animas Vibe Insulin Pump and Blood Glucose Analyser - ongoing issues with screen fade, cracked battery casing and other issues. 24 March 2017. Reports of issues with these devices have been received by Medsafe. The reports predominantly relate to issues with screen fade or cracked battery casing.
