Baxter International issued an urgent device correction Oct. 29 related to all of its Spectrum infusion pumps. The devicemaker said that deviations from specific cleaning methods may impair the pumps’ ...

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 US Food and Drug Administration (FDA) has issued an early alert over a ‘potentially high-risk’ issue with certain Baxter Sigma Spectrum and Spectrum IQ infusion pumps. The agency’s notice ...

Baxter Healthcare has issued a recall for some Spectrum infusion pumps due to a potential defect involving missing motor mounting screws, which could lead to interruptions, delays or incorrect dosing ...

Errors in the setup or management of some of Baxter International’s infusion pumps could result in overlooked blockages in the pumps, potentially leading to serious injury or even death, the ...

Baxter International Inc. announced today it has issued an Urgent Medical Device Correction for all Spectrum IQ infusion pumps to reinforce important safety information when customers implement ...