FDAClass IIMay 22, 2024

Spectrum IQ Infusion pump recall

Spectrum IQ Infusion pump, Product Code 357009

Why was Spectrum IQ Infusion pump recalled?

There is a potential for cracks on the mount of the front panel of the device.

What should I do if I have this product?

The recall is ongoing. Follow the firm and FDA instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

UDI/DI 00085412610900, Serial Numbers: 3770692, 3770755, 3770781, 3770816, 3770932, 3771122, 3771364, 3771374, 3771419

Product
Spectrum IQ Infusion pump, Product Code 357009
Recalling firm
Baxter Healthcare Corporation
Quantity
9 units
Distribution
US Nationwide distribution in the states of Ohio, Wisconsin.
Recall date
May 22, 2024
Classification
Class II
Status
Ongoing
Agency
FDA (device)
Open FDA enforcement record Latest recalls