FDA-Device2024-05-15Class II
Baxter Spectrum IQ Infusion Pump, Product Code 3570009
Hazard
One device was improperly performed testing prior to release from a Service Center.
Sold states
US Nationwide distribution in the state of Massachusetts.
Affected count
1 pump
Manufactured in
1 Baxter Pkwy, N/A, Deerfield, IL, United States
Products
Baxter Spectrum IQ Infusion Pump, Product Code 3570009
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1775-2024More Baxter Healthcare Corporation recalls
- FDA-Device2026-07-08Hillrom VOLARA System P.CIRCUIT KIT AC recalled for nebulizer cup leakage risk
- FDA-Device2026-07-08Baxter operating table head positioning adapter recalled for loosening risk
- FDA-Device2026-07-08Hillrom VOLARA System P.CIRCUIT 5KIT AC recalled for nebulizer cup leakage risk
- FDA-Device2026-07-08Hillrom VOLARA System P.CIRCUIT KIT recalled for nebulizer cup leakage risk
- FDA-Device2026-07-08Hillrom Volara P.Circuit 5Kit breathing device recalled for nebulizer cup leakage risk
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