Class II — Baxter Healthcare Corporation
| Recalling firm | BAXTER HEALTHCARE CORPORATION |
|---|---|
| Registered facility | View this company's 32 registered facilities → (openFDA recall records do not name a specific facility) |
| Classification | Class II |
| Status | Ongoing |
| Reason | There is a potential for cracks on the mount of the front panel of the device. |
| Product | Spectrum IQ Infusion pump, Product Code 357009 |
| Quantity | 9 units |
| Distribution | US Nationwide distribution in the states of Ohio, Wisconsin. |
| Initiated | 2024-04-09 |
| Classified | 2024-05-13 |
| Recall number | Z-1810-2024 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Baxter Healthcare Corporation (Z-1810-2024).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/94451/
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