Baxter recalls Spectrum IQ Infusion Pumps with Product Code 3570009 due to potential grease breakdown causing premature wear and ineffective therapy. Affected units have specific serial numbers.
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.
Baxter is recalling Spectrum IQ Infusion Pumps with Product Code 3570009 because certain units may have been manufactured with grease that breaks down quickly. This could cause the pump to wear out prematurely and deliver ineffective therapy.
The pump may have been manufactured with grease that breaks down quickly. This breakdown can cause the pump's mechanism to wear out prematurely, leading to ineffective therapy delivery.
Patients using the Spectrum IQ Infusion Pump with Product Code 3570009 are affected. Those with specific serial numbers listed in the recall are most at risk.
Check for Product Code 3570009 on the pump. Affected units have specific serial numbers: 3815255, 3815261, 3815265, 3815266, 3815267, 3815271.
Verify the product code on your pump is 3570009.
Compare your pump's serial number to the list: 3815255, 3815261, 3815265, 3815266, 3815267, 3815271.
Baxter identified that certain pumps may have been manufactured with grease that breaks down quickly, potentially causing premature wear and ineffective therapy.
Check the product code and serial numbers to see if your pump is affected. If it is, contact Baxter for further instructions.
The recall record does not mention a remedy or fix.
We’ve drafted a message you can send Baxter to request your refund or repair — edit it as you like.
Subject: Recall Z-2415-2025 — Baxter Baxter Hello, I own a Baxter that is covered by recall Z-2415-2025 from Baxter. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
