Baxter Sigma Spectrum Infusion System (V6 Platform), Product Code 35700BAX
Reported: March 12, 2025 Initiated: February 5, 2025 #Z-1253-2025
Product Description
Baxter Sigma Spectrum Infusion System (V6 Platform), Product Code 35700BAX
Reason for Recall
There is the potential for missing motor mounting screws, which may have occurred during the servicing process.
Details
- Recalling Firm
- Baxter Healthcare Corporation
- Units Affected
- 66 units
- Distribution
- US: Nationwide
- Location
- Deerfield, IL
Frequently Asked Questions
What product was recalled? ▼
Baxter Sigma Spectrum Infusion System (V6 Platform), Product Code 35700BAX. Recalled by Baxter Healthcare Corporation. Units affected: 66 units.
Why was this product recalled? ▼
There is the potential for missing motor mounting screws, which may have occurred during the servicing process.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on March 12, 2025. Severity: Critical. Recall number: Z-1253-2025.
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