Baxter TruSystem 7500 Hybrid Plus: Emergency Mode Causes Back Section Unadjustable
Baxter recalls TruSystem 7500 Hybrid Plus (FC) with software issue where emergency mode makes upper back section unadjustable. Affected units have product code 1854087 and serial numbers up to 11/14/2024.
Use caution until it’s fixed
There is a software issue which causes the upper back section to not be operable/adjustable when the "emergency mode" function is enabled.
Contact the company
What happened, in plain English
Baxter is recalling its TruSystem 7500 Hybrid Plus (FC) medical device due to a software issue that makes the upper back section unadjustable when emergency mode is enabled. This could affect patient safety during critical medical procedures. Read more at govinfonow.com/recall/52749-baxter-trusystem-7500-hybrid-plus-emergency-mode-causes-back-section.
Source Summary by GovInfoNow · govinfonow.com/recall/52749-baxter-trusystem-7500-hybrid-plus-emergency-mode-causes-back-section · Updated August 17, 2026 · FDA enforcement record: FDA #Z-1419-2025
Cite this page
“Baxter TruSystem 7500 Hybrid Plus: Emergency Mode Causes Back Section Unadjustable.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/52749-baxter-trusystem-7500-hybrid-plus-emergency-mode-causes-back-section. Based on FDA recall #Z-1419-2025 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1419-2025%22&limit=1).
Why it’s dangerous
The software issue causes the upper back section to become unadjustable when emergency mode is activated. This could prevent proper adjustment of critical medical equipment during emergencies, potentially affecting patient safety.
Who’s affected
Healthcare facilities using the Baxter TruSystem 7500 Hybrid Plus (FC) device with product code 1854087 are most at risk. Patients receiving care through this equipment could be impacted if the issue occurs during emergency procedures.
How to tell if you have this one
Check for product code 1854087 on the device. Affected units have serial numbers manufactured until November 14, 2024. The device is labeled as "Baxter TruSystem 7500 Hybrid Plus (FC)."
- Brand
Baxter- Category
Medical device
All 14 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
- Classification
Class II- Status
Ongoing- Distribution
US Nationwide distribution.
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| Z-1409-2025 | Baxter Operating table column TS7500 MOBIUS, Product Code 1704695; UID/DI 00887761974425, All serial numbers manufactured until 11/14/2024. | 403 units |
| Z-1410-2025 | Baxter Stationary column TruSystem 7500, Product Code 1717020; UID/DI 00887761974418, All serial numbers manufactured until 11/14/2024. | 462 units |
| Z-1411-2025 | Baxter Floor mounting column TruSystem 7500, Product Code 1717021; UID/DI 00887761974401, All serial numbers manufactured until 11/14/2024. | 112 units |
| Z-1412-2025 | Baxter Mobile column TruSystem 7500, Product Code 1717023; UID/DI 00887761974395, All serial numbers manufactured until 11/14/2024. | 1596 units |
| Z-1413-2025 | Baxter Mobile column TruSystem 7500 U, Product Code 1730720; UID/DI 00887761974388, All serial numbers manufactured until 11/14/2024. | 40 units |
| Z-1414-2025 | Baxter Stationary column TruSystem 7500 U, Product Code 1730731; UID/DI 00887761974371, All serial numbers manufactured until 11/14/2024. | 2 units |
| Z-1415-2025 | Baxter Floor mounting column TS 7500 U, Product Code 1730732; UID/DI 00887761974364, All serial numbers manufactured until 11/14/2024. | 33 units |
| Z-1416-2025 | Baxter TruSystem 7500 Hybrid (MC), Product Code 1773204; UID/DI 00887761974326, All serial numbers manufactured until 11/14/2024. | 2 units |
| Z-1417-2025 | Baxter TruSystem 7500 Hybrid (FC), Product Code 1854085; UID/DI 00887761974081, All serial numbers manufactured until 11/14/2024. | 10 units |
| Z-1418-2025 | Baxter TruSystem 7500 Hybrid (SC), Product Code 1854086; UID/DI 00887761974074, All serial numbers manufactured until 11/14/2024. | 8 units |
| Z-1419-2025 | Baxter TruSystem 7500 Hybrid Plus (FC), Product Code 1854087; UID/DI 00887761974067, All serial numbers manufactured until 11/14/2024. | 93 units |
| Z-1420-2025 | Baxter TruSystem 7500 Hybrid Plus (SC), Product Code 1854088; UID/DI 00887761974050, All serial numbers manufactured until 11/14/2024. | 48 units |
| Z-1421-2025 | Baxter TruSystem 7500 Hybrid MR IMRIS, Product Code 2067886; UID/DI 00887761973763, All serial numbers manufactured until 11/14/2024. | 24 units |
| Z-1422-2025 | Baxter TruSystem 7500, Product Code 4091000; UID/DI 00887761968639, All serial numbers manufactured until 11/14/2024. | 1709 units |
What to do — step by step
Check Device Status
Verify if emergency mode activation makes the upper back section unadjustable.
Where it went and when
Where it was distributed
Distributed nationwide.
FDA distribution: “US Nationwide distribution.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA published this recall 36 days after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #Z-1419-2025 (February 25, 2025) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1419-2025 to see it in context.
- Plain-language summary written by qwen3:4b on August 17, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.