FDA Device recall Z-2999-2026
Medline medical convenience kit labeled as: TRACH TUBE KIT, Medline Kit SKU DYKM2330
- FDA Device
- Class II
- ongoing
- Published 2026-09-02
On 2026-09-02 the FDA classified a Class II recall of Medline medical convenience kit labeled as: TRACH TUBE KIT, Medline Kit SKU DYKM2330 by Medline Industries, citing component labeling discrepancy.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2999-2026 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2026-07-10 |
| Published | 2026-09-02 |
| Last updated | 2026-09-13 11:58 UTC |
| Company | Medline Industries |
| Distribution | US |
Product
Medline medical convenience kit labeled as: TRACH TUBE KIT, Medline Kit SKU DYKM2330
Reason
Component labeling discrepancy
Identifiers
| code_info | UDI/DI 10198459582158 (each) 40198459582159 (case), Lot Number 26FLA408 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:58 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2999-2026%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.