FDA Device recall Z-1775-2024
Baxter Spectrum IQ Infusion Pump, Product Code 3570009
- FDA Device
- Class II
- ongoing
- Published 2024-05-15
On 2024-05-15 the FDA classified a Class II recall of Baxter Spectrum IQ Infusion Pump, Product Code 3570009 by Baxter Healthcare, citing one device was improperly performed testing prior to release from a Service Center.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1775-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2024-03-20 |
| Published | 2024-05-15 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Baxter Healthcare |
| Distribution | US |
Product
Baxter Spectrum IQ Infusion Pump, Product Code 3570009
Reason
One device was improperly performed testing prior to release from a Service Center.
Identifiers
| code_info | UDI/DI 00085412610900, Serial Number 3540772 |
|---|
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-1775-2024%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.