The Recall Desk

FDA (Devices) recall action 96289

Baxter Healthcare Corporation recalled 2 products on 2025-03-12

The FDA (Devices) publishes a recall like this one as 2 separate product records. They share a firm, a date and a cause; this page is all of them in one place, so the scale of the action is visible rather than spread across 2 pages.

Products
2
Announced
2025-03-12
Critical
0
Units
389

Why these products were recalled

There is the potential for missing motor mounting screws, which may have occurred during the servicing process.

The agency’s own wording, quoted from the enforcement report.

The unit total adds up the quantities the agency stated for each product. Where a product record gave no figure, or gave a weight rather than a count, it contributes nothing — so the real total is at least this, never less.

1–2 of 2

  • SevereFDA (Devices)··2025-03-12

    Baxter Spectrum IQ Infusion System may have missing motor mounting screws

    Baxter Spectrum IQ Infusion Systems may lack motor mounting screws due to a servicing defect. The FDA Class I recall affects 323 units distributed nationwide.

    Product
    Baxter Spectrum IQ Infusion System with Dose IQ Safety Software, Product Code 3570009
    Category
    Distribution
    0 states
  • SevereFDA (Devices)··2025-03-12

    Baxter Sigma Spectrum Infusion System Recalled for Missing Mounting Screws

    Baxter Healthcare is recalling 66 units of Sigma Spectrum Infusion System (V6) due to potential missing motor mounting screws that may have occurred during servicing. Missing screws could affect the device's operation.

    Product
    Baxter Sigma Spectrum Infusion System (V6 Platform), Product Code 35700BAX
    Category
    Distribution
    0 states