Baxter Spectrum IQ Infusion Pump Recall: Defective Power Adapter May Fail Over Time

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Contact the company & request your remedy

Recalling firmBaxter Healthcare Corporation711 Park Ave, N/A · Medina, NY 14103-1036

No email on file — write to the address above instead.

✎ GovInfoNow plain-language explainer

What happened, in plain English

Baxter is recalling Spectrum IQ infusion pumps with specific serial numbers because a component in the AC power adapter could fail over time. This could lead to the pump not working properly during fluid administration.

Why it’s dangerous

The AC power adapter in the pump may fail over time, potentially causing the pump to stop working properly. This could lead to improper fluid administration if the pump is not functioning correctly.

Who’s affected

Patients using Baxter Spectrum IQ infusion pumps with the listed serial numbers are affected. Healthcare providers and caregivers who use these pumps are at risk if they have the recalled units.

How to tell if you have this one

Check the serial number on your Spectrum IQ infusion pump. The affected units have specific serial numbers listed in the recall notice.

Brand
Baxter
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Serial Number
Look for the serial number on your pump's label to confirm if it's in the list of affected units.

✎ GovInfoNow

Questions people ask

Why is this pump being recalled?

The recall is due to a potentially defective component in the AC power adapter that may fail over time, which could cause the pump to stop working properly.

How do I know if my pump is affected?

Check the serial number on your pump's label against the list of affected serial numbers provided in the recall notice.

What should I do if my pump is affected?

The recall does not specify a remedy, so contact Baxter Healthcare Corporation directly for further instructions.

Take action

Contact Baxter

We’ve drafted a message you can send Baxter to request your refund or repair — edit it as you like.

✉️ Open in email

Subject: Recall Z-1487-2021 — Baxter Baxter

Hello,

I own a Baxter that is covered by recall Z-1487-2021 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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Where this comes from

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.

Official source: FDA Recall #Z-1487-2021 (March 19, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1487-2021 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.

Baxter Healthcare Corporation recalls Spectrum IQ - Infusion Pump - Product Usage: intended to be used for the controlled administration of fluids.

Lower-risk recall