Baxter Spectrum IQ Infusion Pump — Class II medical device recall Z-1775-2024
Ongoing recall by Baxter Healthcare Corporation, reported 2024-05-15, distributed nationwide. One device was improperly performed testing prior to release from a Service Center.
| Recall number | Z-1775-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Baxter Healthcare Corporation, Deerfield, IL, United States |
| Recall initiated | 2024-03-20 |
| Classified | 2024-05-03 |
| Reported by FDA | 2024-05-15 |
| Distributed | Nationwide (US) |
| Quantity | 1 pump |
| UPC / GTIN / UDI-DI | 00085412610900 |
| Serial numbers | 3540772 |
Product
Baxter Spectrum IQ Infusion Pump, Product Code 3570009
Reason for recall
One device was improperly performed testing prior to release from a Service Center.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1775-2024. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.