Medscape

Sigma Expands Recall of Infusion Pump

June 15, 2012 — Sigma International General Medical Apparatus has expanded an earlier recall of its Spectrum model 35700 infusion pumps because of their tendency to fail suddenly without issuing an ...
Medscape

Class I Recall of Certain Medtronic Infusion Pumps

September 13, 2011 — A class I recall has been issued for certain Medtronic implantable programmable infusion pumps (SynchroMed II), the US Food and Drug Administration (FDA) announced yesterday.
RAPS

Infusion Pump Maker Warned About Alarm Problems

The U.S. Food and Drug Administration (FDA) issued a warning letter to Hospira, Inc., about problems with alarm systems in its infusion pumps, according to a Reuters report. Hospira said the letter ...
RAPS

Tired of Problems With Infusion Pumps, FDA is Trying to Make Them Safer

US regulators have finalized a new set of recommendations intended to make infusion pumps safer and more reliable. In the US, medical devices can come to market in a variety of different ways. Some ...
AOL

Yet another FDA Class 1 recall for Minnesota-made infusion syringe pumps

The U.S. Food and Drug Administration issued a Class I recall, the agency's most serious, for the Medfusion syringe pump, the third major FDA recall for the line of devices made in Oakdale. Smiths ...