FDAJune 5, 2025device

Custom Tubing Kit: REF: K04-00417, K04-00963, K04-01029

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

008844500466300088445004676000884450148938

Recall history

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

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