Official recall record
Spectrum IQ Infusion Pump, Product Code 3570009
- Issuing authority
- US FDA — Medical Devices
- Recall initiated by firm
- 2025-07-14
- Country of alert
- United States
- Alert level
- Class II
- Alert type
- recall
- Barcode (EAN/GTIN)
- 00085412610900
- Brand on record
- Baxter Healthcare Corporation
What the authority reported
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
Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.
Record last checked against the registry on 2026-05-31.
Same barcode in other registries
The same EAN appears in 6 other official recall record(s) — a cross-border signal worth checking if you bought this product abroad.
- 2024-10-02 · US FDA — Medical Devices
Baxter Spectrum IQ Infusion System with Dose IQ Safety Software, Product Code 3570009 - 2018-09-18 · US FDA — Medical Devices
SPECTRUM IQ INFUSION SYSTEM WITH DOSE IQ SAFETY SOFTWARE, 3570009 - 2021-12-29 · US FDA — Medical Devices
Baxter Spectrum IQ Infusion Pumps, Product code 3570009. - 2023-06-15 · US FDA — Medical Devices
The Spectrum IQ Infusion System with Dose IQ Safety Software, Product Code 3570009 - 2026-01-13 · US FDA — Medical Devices
Brand Name: Spectrum IQ Product Name: Infusion Pump Model/Catalog Number: 3570009 Software Version: N/A Product Desc
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All 43 official recall notices naming Baxter Healthcare Corporation on this site →