Recall Ledger

Brand Name: Spectrum IQ Product Name: Infusion Pump Model/Catalog Number: 3570009 ... recall (Baxter Healthcare Corporation)

Medical deviceClass IIOngoing

Summary: Baxter Healthcare Corporation is recalling Brand Name: Spectrum IQ Product Name: Infusion Pump Model/Catalog Number: 3570009 Software Version: N/A Product Description: Infusion Pump, one unit per carton Component: N/A. Reason: Pumps were released without full testing being performed, including occlusion alarm testing.

What is being recalled

Brand Name: Spectrum IQ Product Name: Infusion Pump Model/Catalog Number: 3570009 Software Version: N/A Product Description: Infusion Pump, one unit per carton Component: N/A

Why

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

How serious is it

Class II is the middle level: using or being exposed to this product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.

Where it was sold

States: Ohio Countries: United States (states named: Ohio)

How to tell if yours is affected

Lot Code: GTIN 00085412610900, Serial Numbers 3815663, 3823468, 3824743, 3825234, and 3825599

What to do

Check the model, lot or serial numbers above against your device. If yours is affected, contact the manufacturer or your healthcare provider before you stop using a device you rely on.

Recall facts

Recall numberZ-1368-2026
CategoryMedical device
AgencyU.S. Food and Drug Administration (FDA)
SeverityClass II
StatusOngoing
Recall startedJanuary 13, 2026
ReportedFebruary 25, 2026
CompanyBaxter Healthcare Corporation
Company locationDeerfield, IL, United States
Initiated byVoluntary: Firm initiated
Quantity5

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