Spectrum IQ Infusion Pump recall
Spectrum IQ Infusion Pump, Product Code 3570009
Why was Spectrum IQ Infusion Pump recalled?
Baxter has identified that certain pumps have potentially been released with the grease applied to the cam and motor gears that will break down quickly. The breakdown of the grease will lead to the device having insufficient or ineffective grease applied to the cam, which could lead to premature wear of the mechanism assembly, resulting in excessive therapy.
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: 3815255 3815261 3815265 3815266 3815267 3815271
- Product
- Spectrum IQ Infusion Pump, Product Code 3570009
- Recalling firm
- Baxter Healthcare Corporation
- Quantity
- 6 units
- Distribution
- US distribution to states of: AZ, FL
- Recall date
- September 3, 2025
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)