FDA Device recall Z-1767-2025
Baxter Novum IQ LVP INFUSION SYSTEM, REF 40700BAXUS
- FDA Device
- Class I
- ongoing
- Published 2025-05-28
On 2025-05-28 the FDA classified a Class I recall of Baxter Novum IQ LVP INFUSION SYSTEM, REF 40700BAXUS by Baxter Healthcare, citing there is a potential for the Novum IQ LVP due to the potential for underinfusion following use of the "standby mode" feature or if the device is powered off with the set loaded.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1767-2025 |
| Classification | Class I |
| Status | ongoing |
| Initiated | 2025-04-24 |
| Published | 2025-05-28 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Baxter Healthcare |
| Distribution | n/a |
Product
Baxter Novum IQ LVP INFUSION SYSTEM, REF 40700BAXUS
Reason
There is a potential for the Novum IQ LVP due to the potential for underinfusion following use of the "standby mode" feature or if the device is powered off with the set loaded.
Identifiers
| code_info | All serial numbers |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1767-2025%22
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