FDA Device recall Z-1810-2024
Spectrum IQ Infusion pump, Product Code 357009
- FDA Device
- Class II
- ongoing
- Published 2024-05-22
On 2024-05-22 the FDA classified a Class II recall of Spectrum IQ Infusion pump, Product Code 357009 by Baxter Healthcare, citing there is a potential for cracks on the mount of the front panel of the device.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1810-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2024-04-09 |
| Published | 2024-05-22 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Baxter Healthcare |
| Distribution | US |
Product
Spectrum IQ Infusion pump, Product Code 357009
Reason
There is a potential for cracks on the mount of the front panel of the device.
Identifiers
| code_info | UDI/DI 00085412610900, Serial Numbers: 3770692, 3770755, 3770781, 3770816, 3770932, 3771122, 3771364, 3771374, 3771419 |
|---|
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-1810-2024%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.