Class II

Medical Device Recall: Medline medical convenience kit labeled as: TRACH TUBE KIT, Medline Kit SKU DYKM2330

Medline Industries, LP · July 10, 2026

Reason for Recall

Component labeling discrepancy

Distribution

US Nationwide distribution in the state of California.

States Affected

NATIONWIDE

Quantity Affected

45 kits

Source: FDA (openFDA Device Enforcement)

Recall number: Z-2999-2026

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.

Medline Industries, LP Medical Device Recall: Medline medical convenience kit labeled as: TRACH TUBE KIT, Medline Kit SKU DYKM2330 | SafeCheck