FDAJuly 14, 2025device
Spectrum IQ Infusion Pump, Product Code 3570009
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
Baxter has identified that certain pumps have potentially been released with the grease applied to the cam and motor gears that will break down quickly. The breakdown of the grease will lead to the device having insufficient or ineffective grease applied to the cam, which could lead to premature wear of the mechanism assembly, resulting in excessive therapy.
What to do
FDA enforcement status: Ongoing
Brands named
baxter healthcarebaxter
UPCs
00085412610900
Recall history
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