FDA Medical devices recall ·
Medline medical convenience kit labeled as: TRACH TUBE KIT… recall
- Recall number
- Z-2999-2026
- Date
- (initiated July 10, 2026)
- Company / brand
- Medline Industries, LP
3 Lakes Dr, Northfield, IL, United States - Category
- Medical devices › Class II
- Classification
- Class II
- Status
- Ongoing
- Units affected
- 45 kits
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
Product
Medline medical convenience kit labeled as: TRACH TUBE KIT, Medline Kit SKU DYKM2330
Why was it recalled?
Component labeling discrepancy
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
UDI/DI 10198459582158 (each) 40198459582159 (case), Lot Number 26FLA408
Distribution
US Nationwide distribution in the state of California.
States: California
What does Class II mean?
Class II means use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or the probability of serious harm is remote.
Source: FDA (medical devices), recall Z-2999-2026. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.