Spectrum IQ Infusion pump — Class II medical device recall Z-1810-2024
Ongoing recall by Baxter Healthcare Corporation, reported 2024-05-22, distributed nationwide. There is a potential for cracks on the mount of the front panel of the device.
| Recall number | Z-1810-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Baxter Healthcare Corporation, Deerfield, IL, United States |
| Recall initiated | 2024-04-09 |
| Classified | 2024-05-13 |
| Reported by FDA | 2024-05-22 |
| Distributed | Nationwide (US) |
| Quantity | 9 units |
| Reason classes | packaging |
| UPC / GTIN / UDI-DI | 00085412610900 |
| Serial numbers | 3770692, 3770755, 3770781, 3770816, 3770932, 3771122, 3771364, 3771374, 3771419 |
Product
Spectrum IQ Infusion pump, Product Code 357009
Reason for recall
There is a potential for cracks on the mount of the front panel of the device.
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-1810-2024. 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.