FDAJune 5, 2025device

Custom Manifold Kit: REF: K09-02239C, K09-02249UP, K09-09110B, K09-10294A, K09-11227A, K09-11456B, K09-12123B, K09-13342AP, K09-13391BP, K09-13548, K09-14000A, K09T-12020D, K09T-12275B

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

High pressure tubing may relax over time causing it to partially separate from the connector resulting in a void that can trap air in the line. Use of the affected product may result in the trapped air being introduced into the patient.

What to do

FDA enforcement status: Ongoing

Brands named

merit medical systemsmeritmerit medical

UPCs

008844502043130088445033004300884450279076008844502100000088445021069700884450279717008844507411460088445054871400884450752111008844505823290088445078510200884450860007

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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