FDA-Device2025-04-02Class II
Baxter TruSystem 7500, Product Code 4091000
Hazard
There is a software issue which causes the upper back section to not be operable/adjustable when the "emergency mode" function is enabled.
Sold states
US Nationwide distribution.
Affected count
1709 units
Manufactured in
1 Baxter Pkwy, N/A, Deerfield, IL, United States
Products
Baxter TruSystem 7500, Product Code 4091000
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1422-2025More 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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