Baxter recalls Spectrum Infusion Pump V8 Model 35700BAX2 with incorrect software version. Affected units may have safety risks; contact for repair or replacement.
Certain Spectrum infusion pumps may have an incorrect version of software.
Baxter is recalling certain Spectrum Infusion Pump V8 models due to a potential software version error. This could affect the pump's safety performance, though the specific risk isn't detailed in the recall notice.
The recall states that certain pumps may have an incorrect software version. This could lead to improper function of the pump, potentially affecting patient safety during infusion therapy. However, the exact risk level is not specified in the recall notice.
Healthcare professionals and patients using the Baxter Spectrum Infusion Pump V8 Model 35700BAX2 are likely affected. Those with the specific serial numbers listed in the recall are at risk.
Check for the model number 35700BAX2 on the pump. Affected units have specific serial numbers listed in the recall notice, including 2006307, 2052091, and others.
Verify the model number on your pump; affected units are the Spectrum Infusion Pump V8 with model number 35700BAX2.
The recall states that certain Spectrum infusion pumps may have an incorrect software version, which could affect safety performance.
The recall does not specify a remedy; you should check the pump model and serial numbers to see if it is affected.
Check the model number on your pump; affected units are the Spectrum Infusion Pump V8 with model number 35700BAX2 and specific serial numbers listed in the recall notice.
We’ve drafted a message you can send Baxter to request your refund or repair — edit it as you like.
Subject: Recall Z-2096-2025 — Baxter Baxter Hello, I own a Baxter that is covered by recall Z-2096-2025 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.
