Baxter recalls Sigma Spectrum Infusion System (V6 Platform) with Product Code 35700BAX due to potential missing motor mounting screws during servicing. Affected units have specific serial numbers.
There is the potential for missing motor mounting screws, which may have occurred during the servicing process.
Baxter is recalling its Sigma Spectrum Infusion System (V6 Platform) because there's a risk of missing motor mounting screws that could occur during servicing. This could lead to improper function of the infusion system if not addressed.
The hazard involves the potential for missing motor mounting screws during servicing. If screws are not properly secured, the motor may not function correctly, which could affect the infusion system's performance.
Healthcare professionals and patients using the Baxter Sigma Spectrum Infusion System (V6 Platform) with Product Code 35700BAX are likely affected. Those who have the specific serial numbers listed in the recall are at the highest risk.
Check if your Baxter Sigma Spectrum Infusion System (V6 Platform) has Product Code 35700BAX and the listed serial numbers. The recall includes specific units with serial numbers starting with 704198 through 1024109.
Verify your device has Product Code 35700BAX and one of the listed serial numbers.
Baxter recalls the Sigma Spectrum Infusion System (V6 Platform) due to potential missing motor mounting screws that could occur during servicing.
Check if your device has Product Code 35700BAX and one of the listed serial numbers. If it does, contact Baxter for further instructions.
The recall states there is a potential for missing motor mounting screws, but no specific risk of serious injury is mentioned in the record.
We’ve drafted a message you can send Baxter to request your refund or repair — edit it as you like.
Subject: Recall Z-1253-2025 — Baxter Baxter Hello, I own a Baxter that is covered by recall Z-1253-2025 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
