Spectrum IQ — Class II medical device recall Z-1487-2021
Terminated recall by Baxter Healthcare Corporation, reported 2021-05-05, distributed nationwide. Potentially defective component in the AC power adapter which may fail over time.
| Recall number | Z-1487-2021 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Baxter Healthcare Corporation, Medina, NY, United States |
| Recall initiated | 2021-03-19 |
| Classified | 2021-04-23 |
| Reported by FDA | 2021-05-05 |
| Terminated | 2022-07-15 |
| Distributed | Nationwide (US) |
| Quantity | 408 units |
| Reason classes | device malfunction |
| Serial numbers | 3008222, 3011477, 3012363, 3013708, 3014132, 3014459, 3500621, 3500772, 3502812, 3522442, 3525471, 3526276, 3526801, 3526869, 3527443, 3527832, 3528039, 3528084, 3528271, 3528426, 3528462, 3528535, 3528601, 3530776, 3530964 and 383 more |
Product
Spectrum IQ - Infusion Pump - Product Usage: intended to be used for the controlled administration of fluids.
Reason for recall
Potentially defective component in the AC power adapter which may fail over time.
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-1487-2021. 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.