FDA Device recall Z-0151-2024
Novum IQ Syringe infusion system, Product Code 40800BAXUS
- FDA Device
- Class I
- ongoing
- Published 2023-11-15
On 2023-11-15 the FDA classified a Class I recall of Novum IQ Syringe infusion system, Product Code 40800BAXUS by Baxter Healthcare, citing baxter is issuing an Urgent Medical Device Correction for the Novum IQ Syringe Pump. Baxter identified that after multiple downstream occlusion alarms, the pump may display an Inf….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0151-2024 |
| Classification | Class I |
| Status | ongoing |
| Initiated | 2023-10-13 |
| Published | 2023-11-15 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Baxter Healthcare |
| Distribution | US |
Product
Novum IQ Syringe infusion system, Product Code 40800BAXUS
Reason
Baxter is issuing an Urgent Medical Device Correction for the Novum IQ Syringe Pump. Baxter identified that after multiple downstream occlusion alarms, the pump may display an Infusion Complete alarm even though uninfused fluid remains in the syringe.
Identifiers
| code_info | All Serial Numbers |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0151-2024%22
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