The Recall Desk

Hazard

Underinfusion recalls

2 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total
2
Critical
1
Severe
1
Most recent
2025-08-20

Of the 2 underinfusion recalls we have scored against our rubric, 1 (50%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1 (50%) are Severe.

About this hazard tag

Hazard tags are short, machine-readable labels we attach to every recall to make cross-cutting queries possible — “all underinfusion recalls regardless of agency”, “all listeria recalls in California”, “all airbag recalls in 2025”. The tags are extracted from each recall’s source text during the LLM rewrite step and validated against a fixed schema.

A recall can carry multiple tags — a Listeria recall might also be tagged ready-to-eat and undeclared-allergen. Use the full-text search if you want to combine hazard tags with brand or category filters.

1–2 of 2

  • CriticalFDA (Devices)·Z-2173-2025·2025-08-20

    Infusion pumps recalled over underinfusion when flow rate more than doubles

    Baxter is issuing an urgent correction for 36,705 Novum IQ large volume pumps because the pump may underinfuse when moving to a flow rate more than double the current one.

    Product
    Baxter Novum IQ Large Volume Pump, Product Code REF 40700BAXUS
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1767-2025·2025-05-28

    Baxter Novum IQ LVP Infusion System underinfusion risk recall

    Baxter Healthcare is recalling the Novum IQ LVP Infusion System because the device may deliver less medication than intended when using standby mode or after being powered off with the set loaded.

    Product
    Baxter Novum IQ LVP INFUSION SYSTEM, REF 40700BAXUS
    Category
    Medical Device
    Distribution
    0 states