Baxter recalls Spectrum Infusion Pump V6 Model 35700BAX with incorrect software version. Affected units may have safety risks; contact Baxter for details.
Certain Spectrum infusion pumps may have an incorrect version of software.
Baxter is recalling certain Spectrum Infusion Pump V6 models (35700BAX) due to a potential software issue. This could affect patient safety during medical treatments.
The pumps may have an incorrect software version that could lead to improper medication delivery. This might cause treatment errors or safety issues during medical procedures.
Patients using these infusion pumps for medical treatments are affected. Healthcare providers and caregivers who use the pumps are most at risk.
Check for the model number 35700BAX on the pump. Affected units have specific serial numbers listed in the recall notice.
Look for the model number 35700BAX on the pump's label.
Reach out to Baxter Healthcare Corporation for further instructions on the recall.
The affected model number is 35700BAX.
Check for the model number 35700BAX and the listed serial numbers in the recall notice.
Contact Baxter Healthcare Corporation for instructions on the recall.
We’ve drafted a message you can send Baxter to request your refund or repair — edit it as you like.
Subject: Recall Z-2095-2025 — Baxter Baxter Hello, I own a Baxter that is covered by recall Z-2095-2025 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.
