Baxter SIGMA Spectrum Infusion Pump, Product Code: 35700BAX2
Reported: August 14, 2024 Initiated: June 14, 2024 #Z-2530-2024
Product Description
Baxter SIGMA Spectrum Infusion Pump, Product Code: 35700BAX2
Reason for Recall
Improperly performed testing prior to release
Details
- Recalling Firm
- Baxter Healthcare Corporation
- Units Affected
- 1 unit
- Distribution
- US Nationwide distribution in the state of Florida.
- Location
- Deerfield, IL
Frequently Asked Questions
What product was recalled? ▼
Baxter SIGMA Spectrum Infusion Pump, Product Code: 35700BAX2. Recalled by Baxter Healthcare Corporation. Units affected: 1 unit.
Why was this product recalled? ▼
Improperly performed testing prior to release
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on August 14, 2024. Severity: Moderate. Recall number: Z-2530-2024.
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