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 ...
Nasdaq

FDA Identifies ICU Medical's Plum Duo Recall as Serious Type

ICU Medical ICUI is currently encountering a recall notice from the FDA for its Plum Duo Infusion System. The recall is for correcting certain devices with software issues, but does not involve ...