Lower risk Medical device recall · FDA · Published January 13, 2026

Spectrum IQ Infusion Pump Recall: Untested Occlusion Alarms May Cause Inaccurate Dosing

Baxter Healthcare recalls Spectrum IQ Infusion Pump model 3570009 due to untested occlusion alarms, which may lead to inaccurate medication dosing. Affected units have specific serial numbers and lot codes.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #Z-1368-2026Medical device Spectrum IQ ›

Lower-risk recall

Pumps were released without full testing being performed, including occlusion alarm testing.

Take action

Contact the company

Recalling firmBaxter Healthcare Corporation1 Baxter Pkwy · Deerfield, IL 60015-4625

✎ GovInfoNow plain-language explainer

Baxter Healthcare is recalling Spectrum IQ Infusion Pumps with model number 3570009 because they were released without full testing, including occlusion alarm testing. This could lead to inaccurate medication dosing if the pump fails to detect blockages in the tubing. Read more at govinfonow.com/recall/50161-spectrum-iq-infusion-pump-recall-untested-occlusion-alarms-may-cause.

Source Summary by GovInfoNow · govinfonow.com/recall/50161-spectrum-iq-infusion-pump-recall-untested-occlusion-alarms-may-cause · Updated August 17, 2026 · FDA enforcement record: FDA #Z-1368-2026

Cite this page

“Spectrum IQ Infusion Pump Recall: Untested Occlusion Alarms May Cause Inaccurate Dosing.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/50161-spectrum-iq-infusion-pump-recall-untested-occlusion-alarms-may-cause. Based on FDA recall #Z-1368-2026 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1368-2026%22&limit=1).

Baxter Healthcare Corporation voluntarily recalled Spectrum IQ Infusion Pump model 3570009 on Jan. 13, 2026, according to the FDA. The pumps were released without full testing, including occlusion alarm testing.

How to tell if you have it

Brand: Spectrum IQ
Product Name: Infusion Pump
Model/Catalog Number: 3570009
UPC: 00085412610900
Lot Code: GTIN 00085412610900
Serial Numbers: 3815663, 3823468, 3824743, 3825234, and 3825599
Sold in Ohio

The hazard

The pumps were released without full testing being performed, including occlusion alarm testing.

Context

GovInfoNow's records show Baxter Healthcare Corporation has 187 other recalls on record since 2015-09-02. Other recent recalls of similar products include Fresenius Kabi Ivenix Infusion Pump Recall (2025-11-03), ICU Medical Plum Solo IV Pump Recall (2026-04-29) and ICU Medical Plum Duo IV Pump Recall (2026-04-29).

How to tell if you have this one

Check for model number 3570009 on the pump. Affected units have serial numbers 3815663, 3823468, 3824743, 3825234, or 3825599 and lot code GTIN 00085412610900.

Brand
Spectrum IQ
Product
Brand Name: Spectrum IQ Product Name: Infusion Pump Model/Catalog Number: 3570009 Software Version: N/A Product
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Serial Numbers
Look for serial numbers 3815663, 3823468, 3824743, 3825234, or 3825599 on the pump.

Where it went and when

Where it was distributed

Distributed in Ohio, and outside the U.S.

FDA distribution: “States: Ohio Countries: United States” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Ohio.

Recall timeline

FDA published this recall 43 days after the firm started it.

Jan 13, 2026Firm started the recall
Feb 13, 2026FDA classified it Class II
Feb 25, 2026Published in FDA’s Enforcement Report

Dates from the agency record only; steps without a date are left out.

Similar recalls

Other Spectrum IQ recalls

Latest medical device recalls

Keep exploring

More Spectrum IQ recalls

Link to this recall

<a href="https://govinfonow.com/recall/50161-spectrum-iq-infusion-pump-recall-untested-occlusion-alarms-may-cause">Spectrum IQ Infusion Pump Recall: Untested Occlusion Alarms May Cause Inaccurate Dosing (GovInfoNow)</a>

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-1368-2026 (January 13, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1368-2026 to see it in context.
Plain-language summary written by qwen3:4b on August 17, 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.