Baxter TruSystem 7500, Product Code 4091000
Reported: April 2, 2025 Initiated: February 25, 2025 #Z-1422-2025
Product Description
Baxter TruSystem 7500, Product Code 4091000
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.
Details
- Recalling Firm
- Baxter Healthcare Corporation
- Units Affected
- 1709 units
- Distribution
- US Nationwide distribution.
- Location
- Deerfield, IL
Frequently Asked Questions
What product was recalled? ▼
Baxter TruSystem 7500, Product Code 4091000. Recalled by Baxter Healthcare Corporation. Units affected: 1709 units.
Why was this product recalled? ▼
There is a software issue which causes the upper back section to not be operable/adjustable when the "emergency mode" function is enabled.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on April 2, 2025. Severity: Moderate. Recall number: Z-1422-2025.
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