Baxter recalls SIGMA Spectrum Infusion Pumps with product code 3570: improper testing before release may cause safety issues. Affected units have serial number 2158913.
Improperly performed testing prior to release
Baxter is recalling SIGMA Spectrum Infusion Pumps with product code 35700BAX2 due to improper testing before release. This could lead to safety risks if the pump is used without proper validation.
The pump was released without proper testing, which could lead to safety issues if used without validation. This might cause improper medication delivery or other complications during medical treatment.
Patients using the Baxter SIGMA Spectrum Infusion Pump with product code 35700BAX2 and serial number 2158913 are affected. Healthcare providers and patients using this specific model are at risk.
Check for product code 35700BAX2 and serial number 2158913 on the pump. This model was sold by Baxter Healthcare Corporation.
Identify the product code and serial number on your pump to confirm if it is affected.
The recall states improper testing before release, but the specific danger is not detailed in the official notice.
Check for product code 35700BAX2 and serial number 2158913 on the pump.
The official notice does not specify a remedy, so contact Baxter Healthcare Corporation 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-2530-2024 — Baxter Baxter Hello, I own a Baxter that is covered by recall Z-2530-2024 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.
