Recall Z-2999-2026— Medline Industries, LP
Class II · Ongoing
Class II FDA medical device recall by Medline Industries, LP, initiated 2026-07-10. FDA's recall record names no specific 510(k) clearance for this event. Product: Medline medical convenience kit labeled as: TRACH TUBE KIT, Medline Kit SKU DYKM2330. Reason: Component labeling discrepancy.
- Recalling firm
- Medline Industries, LP
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2026-07-10
- Firm location
- Northfield, IL, United States
Product description
Medline medical convenience kit labeled as: TRACH TUBE KIT, Medline Kit SKU DYKM2330
Reason for recall
Component labeling discrepancy
Data sourced from openFDA. This site is unofficial and independent of the FDA.