Drug recall
Novum IQ Syringe infusion system, Product Code 40800BAXUS
FDA recall event 93191 · Class I · Baxter Healthcare Corporation
Key facts
| Event ID | 93191 |
|---|---|
| Recall numbers | Z-0151-2024 |
| Recalling firm | Baxter Healthcare Corporation |
| Product type | Devices |
| Products | Novum IQ Syringe infusion system, Product Code 40800BAXUS |
| Classification | Class I |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | 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… |
| Initiation date | Oct 13, 2023 |
| Report date | Nov 15, 2023 |
| City | Deerfield |
| State | IL |
| Country | United States |
| FEI number | 1417572 |
At a glance
- 1–9 Products in this recall
- 10–99 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: