ProductGuru Recalls

Official recall record

Spectrum IQ Infusion Pump, Product Code 3570009

US FDA — Medical Devices · 2025-07-14 · United StatesClass II
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.

Verify at the source: US FDA — Medical Devices — official record →
Record last checked against the registry on 2026-05-31.

More recalls: US FDA — Medical Devices · United States · all filters

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.

Other recalls from this brand

All 43 official recall notices naming Baxter Healthcare Corporation on this site →

ProductGuru Recalls republishes official safety information with attribution. We are not the issuing authority and this page is not advice. If this product is a medical device or medication, speak to a doctor or pharmacist. Found an error? Report it — corrections are published.