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Recall Observatory FDA recall evidence

Device product

Baxter Clearlink System Solution Set with Duo-Vent Spike, REF 2R8538

Z-1010-2025

December 20, 2024

Class II

Product summary

Firm
Baxter Healthcare Corporation
Event
Event 95929
Status
Ongoing
Classification
Class II
Quantity
Unavailable
Official record key
device-enforcement:Z-1010-2025

Official wording

Reason: Specific lots of Solution Sets with Duo-Vent Spike have the potential for inverted side clamps causing the tubing to be unusable.

Code information: UDI/DI 00085412676647, Lot Numbers: DR24C15109 (exp. 3/16/2026)

Distribution pattern: US Nationwide distribution in the states of MN, MO, VA, TX, CA, MA, FL, SC.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Specific lots of Solution Sets with Duo-Vent Spike have the potential for inverted side clamps causing the tubing to be unusable.