Class II

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

MEDLINE INDUSTRIES, LP - Northfield · January 9, 2025

Reason for Recall

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.

Distribution

US States: CA, NY

States Affected

CA, NY

Quantity Affected

70 kits

Source: FDA (openFDA Device Enforcement)

Recall number: Z-1182-2025

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.