Baxter recalls Spectrum IQ Infusion Systems with Dose IQ Safety Software (Product Code 3570009) due to potential missing motor mounting screws during servicing, which could affect device safety.
There is the potential for missing motor mounting screws, which may have occurred during the servicing process.
Baxter is recalling its Spectrum IQ Infusion System with Dose IQ Safety Software (Product Code 3570009) because there's a risk of missing motor mounting screws during servicing. This could lead to improper device function, but the recall doesn't specify a direct safety hazard like injury or fire.
The hazard occurs if motor mounting screws are missing during servicing, which could cause the device to malfunction. This might lead to incorrect medication delivery or device failure, but the recall does not specify a direct risk of injury or serious harm.
Patients using medical infusion systems with the Baxter Spectrum IQ Infusion System (Product Code 3570009) are likely affected. Healthcare providers who service these devices may be at higher risk if screws are missing.
Check for the Product Code 3570009 on the device. Serial numbers listed in the recall include many numbers starting with 3020290 through 3708695. The device has a UDI/DI code of 00085412610900.
Inspect the motor mounting area for any missing screws. If found, stop using the device immediately.
The recall states there is a potential for missing motor mounting screws during servicing, but it does not indicate that the product is dangerous if used correctly.
Check the product code (3570009) and serial numbers listed in the recall, which include many numbers starting with 3020290 through 3708695.
The recall does not specify a remedy for missing screws. If you find missing screws, stop using the device immediately and contact Baxter for further instructions.
We’ve drafted a message you can send Baxter to request your refund or repair — edit it as you like.
Subject: Recall Z-1254-2025 — Baxter Baxter Hello, I own a Baxter that is covered by recall Z-1254-2025 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.
