FDAJanuary 9, 2025device

Medline Convenience Kits for Various Procedures: 1) ADULT INTUBATION TRAY, Model Number DYNJAA254A; 2) ADULT MAIN DISP. INTUB PART A, Model Number DYNJAA262A

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

The hazard

Kits contain recalled components due to reports of reduced skin barrier wear time. This refers to a shorter duration that a skin barrier can effectively adhere to and protect the skin before it needs to be replaced.

What to do

FDA enforcement status: Ongoing

Brands named

medline industries lp northfieldmedlinemedline industries

UPCs

10195327686260401953276862611019532720817240195327208173

Recall history

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

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