Baxter Spectrum IQ Infusion Pump recall
Baxter Spectrum IQ Infusion Pump, Product Code 3570009
Why was Baxter Spectrum IQ Infusion Pump recalled?
One device was improperly performed testing prior to release from a Service Center.
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 Number 3540772
- Product
- Baxter Spectrum IQ Infusion Pump, Product Code 3570009
- Recalling firm
- Baxter Healthcare Corporation
- Quantity
- 1 pump
- Distribution
- US Nationwide distribution in the state of Massachusetts.
- Recall date
- May 15, 2024
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)