Baxter recalls Spectrum IQ Infusion Systems with Dose IQ Safety Software due to potential programming errors. Affected units may have safety risks during fluid administration.
There is a potential software error during programming.
Baxter is recalling its Spectrum IQ Infusion Systems with Dose IQ Safety Software because of a potential software error during programming. This could affect the safe administration of fluids in medical settings.
The software error during programming could lead to incorrect fluid administration settings. This might cause unsafe treatment outcomes if the system fails to properly adjust doses during use.
Healthcare providers using the Baxter Spectrum IQ Infusion System with Dose IQ Safety Software for controlled fluid administration are most at risk. Patients receiving treatments through this system may be affected if the software error occurs.
Check for the product code 3570009 or GTIN 00085412610900 on the device. The system is intended for controlled fluid administration in medical settings.
Look for product code 3570009 or GTIN 00085412610900 on the device.
The recall states there is a potential software error during programming, but the exact risk level is not specified.
The recall does not provide specific action steps beyond checking product details.
Check for product code 3570009 or GTIN 00085412610900 on the device.
We’ve drafted a message you can send Baxter to request your refund or repair — edit it as you like.
Subject: Recall Z-0715-2021 — Baxter Baxter Hello, I own a Baxter that is covered by recall Z-0715-2021 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.
