Spectrum IQ Infusion System (Baxter) – Door Closure Malfunction (2024)
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Baxter Spectrum IQ Infusion System with Dose IQ Safety Software, Product Code 3570009
Brand
Baxter Healthcare Corporation
Lot Codes / Batch Numbers
00085412610900, Serial Numbers: 3796578, 3797382, 3797464, 3797578, 3797728, 3797733, 3798019, 3798200
Products Sold
00085412610900, Serial Numbers: 3796578, 3797382, 3797464, 3797578, 3797728, 3797733, 3798019, 3798200
Baxter Healthcare Corporation is recalling Baxter Spectrum IQ Infusion System with Dose IQ Safety Software, Product Code 3570009 due to The door on the Spectrum IQ Infusion pump may not be able to fully close.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The door on the Spectrum IQ Infusion pump may not be able to fully close.
Recommended Action
Per FDA guidance
Baxter Healthcare notified its consignees on 10/03 and 04/2024 via telephone. The call included information regarding the problem with the device, risk to health, and requested the affected units be removed from service pending inspection. On-site inspections to assess for impact and offer replacement, were scheduled.
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 noticeDistribution
As reported by FDA
GA, ID
Page updated: Jan 10, 2026