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device recall
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Baxter Healthcare Corporation device recall (Cls II)

July 14, 2025updated 5mo ago
community read0 votes

Spectrum IQ Infusion Pump, Product Code 3570009 — Reason: 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. — Status: Ongoing

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same company · ±60 days · 6

  • device recallBaxter Healthcare Corporation device recall (Cls I)Jul 14, 2025
  • device pmaBaxter Healthcare Corporation — Preveleak Surgical Sealant (PMA supplement)Jul 10, 2025
  • device 510kBaxter Healthcare Corporation — Spectrum IQ Infusion System with Dose IQ Safety Software (3570009) (510k cleared)Jul 28, 2025
  • device pmaBaxter Healthcare Corp — FLOSEAL MATRIX/FLOSEAL MATRIX HEMOSTATIC SEALANT/PROCEED HEMOSTATIC SEALANT (PMA supplement)Jun 30, 2025
  • device 510kBaxter Healthcare Corporation — SIGMA Spectrum Infusion Pump with Master Drug Library (510k cleared)Jul 28, 2025
  • device recallBaxter Healthcare Corporation device recall (Cls I)Aug 4, 2025

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