Baxter TruSystem 7500 Hybrid — Class II medical device recall Z-1418-2025
Ongoing recall by Baxter Healthcare Corporation, reported 2025-04-02, distributed nationwide. There is a software issue which causes the upper back section to not be operable/adjustable when the "emergenc
| Recall number | Z-1418-2025 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Baxter Healthcare Corporation, Deerfield, IL, United States |
| Recall initiated | 2025-02-25 |
| Classified | 2025-03-21 |
| Reported by FDA | 2025-04-02 |
| Distributed | Nationwide (US) |
| Quantity | 8 units |
| Reason classes | software |
| UPC / GTIN / UDI-DI | 00887761974074 |
Product
Baxter TruSystem 7500 Hybrid (SC), Product Code 1854086
Reason for recall
There is a software issue which causes the upper back section to not be operable/adjustable when the "emergency mode" function is enabled.
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-1418-2025. 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.