Infusion Pump Recall: Baxter Spectrum IQ Infusion Pump
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 |
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.
How to identify the recalled item
| Lot / date codes | UDI-DI: 00085412610900; Serial Numbers: 3815255 3815261 3815265 3815266 3815267 3815271 |
|---|---|
| Lot / date codes | Lot #: G171359, expiry: 05/31/2027 |
These are the identifiers FDA published for this recall. Most recall notices list no UPC or model number at all — if the code on your item is not shown here, that does not mean the item is excluded. Check the official notice, or contact the company.
Other infusion pump recalls
- Infusion Pump Recall: Tandem t:slim X2 · 2026-04-01
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.