Baxter Healthcare Corporation Baxter Spectrum IQ Infusion Pump, Product Code 3570009 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Baxter Spectrum IQ Infusion Pump, Product Code 3570009
Brand
Baxter Healthcare Corporation
Lot Codes / Batch Numbers
UDI/DI 00085412610900, Serial Number 3540772
Products Sold
UDI/DI 00085412610900, Serial Number 3540772
Baxter Healthcare Corporation is recalling Baxter Spectrum IQ Infusion Pump, Product Code 3570009 due to One device was improperly performed testing prior to release from a Service Center.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
One device was improperly performed testing prior to release from a Service Center.
Recommended Action
Per FDA guidance
The affected customer was contacted via on-site visit on March 20, 2024, and by phone call on March 22, 2024. Baxter has asked the customer to locate the affected pump at their facility and return the device to Baxter for testing.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026