Z-2999-2026 Class II Ongoing
FDA device recall Z-2999-2026 was initiated by Medline Industries, LP on July 10, 2026 and is designated Class II. Reason for recall: Component labeling discrepancy The recall status is ongoing. Affected quantity: 45 kits.
Recall Details
- Product Type
- Devices
- Report Date
- September 2, 2026
- Initiation Date
- July 10, 2026
- Termination Date
- N/A
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 45 kits
Product Description
Medline medical convenience kit labeled as: TRACH TUBE KIT, Medline Kit SKU DYKM2330
Reason for Recall
Component labeling discrepancy
Distribution Pattern
US Nationwide distribution in the state of California.
Code Information
UDI/DI 10198459582158 (each) 40198459582159 (case), Lot Number 26FLA408