Baxter recalls Spectrum IQ Infusion Pumps with Product Code 3570009 due to improper testing before release from a Service Center. Affected units may have safety risks.
One device was improperly performed testing prior to release from a Service Center.
Baxter is recalling Spectrum IQ Infusion Pumps with Product Code 3570009 because one device was improperly tested before being released from a Service Center. This could potentially lead to safety issues if the pump is used without proper testing.
The hazard involves a device that was improperly tested prior to release from a Service Center. This could mean the pump may not function correctly, potentially causing safety issues during use.
Healthcare professionals and patients using Baxter Spectrum IQ Infusion Pumps with Product Code 3570009 are affected. Those who have the specific product code are at risk.
Check for Product Code 3570009 on the pump. The pump also has a UDI/DI number of 00085412610900 and a Serial Number 3540772.
Verify the product code on your pump to see if it matches 3570009.
The pump was improperly tested before release from a Service Center, which could lead to safety issues.
Check the product code on your pump; if it matches 3570009, contact Baxter for further instructions.
The recall record does not specify a deadline for action.
We’ve drafted a message you can send Baxter to request your refund or repair — edit it as you like.
Subject: Recall Z-1775-2024 — Baxter Baxter Hello, I own a Baxter that is covered by recall Z-1775-2024 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.
