Baxter Clearlink System Solution Set with Duo-Vent Spike, REF 2R8538
Reported: January 29, 2025 Initiated: December 20, 2024 #Z-1010-2025
Product Description
Baxter Clearlink System Solution Set with Duo-Vent Spike, REF 2R8538
Reason for Recall
Specific lots of Solution Sets with Duo-Vent Spike have the potential for inverted side clamps causing the tubing to be unusable.
Details
- Recalling Firm
- Baxter Healthcare Corporation
- Distribution
- US Nationwide distribution in the states of MN, MO, VA, TX, CA, MA, FL, SC.
- Location
- Deerfield, IL
Frequently Asked Questions
What product was recalled? ▼
Baxter Clearlink System Solution Set with Duo-Vent Spike, REF 2R8538. Recalled by Baxter Healthcare Corporation.
Why was this product recalled? ▼
Specific lots of Solution Sets with Duo-Vent Spike have the potential for inverted side clamps causing the tubing to be unusable.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on January 29, 2025. Severity: Moderate. Recall number: Z-1010-2025.
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