PlainRecalls
FDA Devices Moderate Class II Ongoing

Baxter Continu-Flo Solution Set with Duo-Vent Spike, REF UC8519

Reported: January 29, 2025 Initiated: December 20, 2024 #Z-1011-2025

Product Description

Baxter Continu-Flo Solution Set with Duo-Vent Spike, REF UC8519

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

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 Continu-Flo Solution Set with Duo-Vent Spike, REF UC8519. 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-1011-2025.