The Food and Drug Administration, stepping up its investigation into defects of medication-delivery pumps made by Baxter International Inc., has seized nearly 7,000 devices distributed from two of the ...
As predicted, not long after Baxter International issued an urgent safety communication about an issue with some of its Spectrum infusion pumps, it has been upgraded to a full-blown recall complete ...
Device manufacturer Baxter released an Urgent Safety Communication last week about the company's Spectrum V8 and Spectrum IQ infusion pumps, citing potential compromised medication delivery caused by ...
For the third time in the last two years, Baxter has been hit with the FDA’s most serious label for a recall affecting its infusion pump systems. This time around, the Class I recall notice is linked ...
The Food and Drug Administration ordered Baxter International to recall all of its Colleague infusion pumps in use and provide a refund or no-cost replacement to United States customers. Electronic ...
Data shared in collaboration with The University of Texas Medical Branch, representing an analysis of more than one million intravenous (IV) infusions using Baxter’s Spectrum IQ large volume infusion ...
Duluth, Minn.-based St. Luke’s Health System implemented Meditech’s smart pump infusion integration into its Baxter Spectrum IQ infusion system so that the health system’s medical records and IV pumps ...
The Food and Drug Administration ordered Baxter International to recall all of its Colleague infusion pumps in use and provide a refund or no-cost replacement to United States customers. Electronic ...
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