Following more than 100 incident reports and three patient injuries, the FDA has announced a Baxter Sigma Spectrum infusion pump recall, warning that false alarms caused by a software upgrade…
The Baxter Clearlink Basic Solution Sets recall comes after dozens of reports of leaks, which could expose patients and doctors to potentially toxic drug cocktails.
Problems with Volara home oxygen systems can lead to lung damage and oxygen deficiency, the FDA and the manufacturer warn.
Baxter has recalled more than 277,000 Sigma Spectrum infusion pumps following three deaths and dozens of serious injuries due to the failure of an alarm that is supposed to warn…
Baxter has issued a warning about problems with some of its Spectrum infusion pumps following reports of injuries and deaths.
Software problems have led to a recall of Baxter Spectrum IQ infusion pumps, which may develop an error which could stop the delivery of life-saving drugs to patients.
More than half a million infusion pumps have been recalled due to the risk of corrosion and delays in treatment.
Improper cleaning of Baxter's Sigma Spectrum infusion pumps has resulted in at least 16 severe injuries, according to an FDA class I recall notice.
Several batches of Baxter Vascu-Guard patches have been recalled following reports of strokes and blood clots because users did not know which side of the patch to apply.
Particulate matter contamination has led to a recall of two lots of Baxter DIANEAL dialysis solution.
