Infusion Pump Recall: Baxter Spectrum IQ Infusion Pump
Announced 2026-02-04 · FDA
Recall issued for Baxter Spectrum IQ Infusion Pump, Product Code 3570009. Some pumps were released with grease on cam and motor gears that can degrade, resulting in insufficient lubrication, premature wear of the mechanism, and potential excessive therapy. Six units distributed in the US (Arizona and Florida) are affected; FDA recall number UDI-DI: 00085412610900; Serial Numbers: 3815255, 3815261, 3815265, 3815266, 3815267, 3815271.
| Brand | Baxter Healthcare Corporation |
|---|---|
| Product | 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. |
| Severity | moderate |
| Units affected | 125496 |
| Distribution | US distribution to states of: AZ, FL |
| Agency | FDA |
| Recall / campaign no. | UDI-DI: 00085412610900; Serial Numbers: 3815255 3815261 3815265 3815266 3815267 3815271 |
WHAT YOU SHOULD DO
- Stop using the affected infusion pumps and set them aside.
- Contact Baxter Healthcare Corporation or your healthcare provider for instructions on inspection, repair, or replacement using the recall details.
- If you own or operate a possibly affected device, provide its serial number to Baxter or your healthcare provider to confirm eligibility.
- Monitor device performance and report any concerns to your healthcare provider or Baxter.
Other Baxter Healthcare Corporation recalls
This is an automatically maintained record of an official recall notice. Details can change; always follow the official notice linked above. See all records in the Recall Database.