FDA recall, , Moderate risk
Medline Trach Tube Kit
The Medline medical convenience kit labeled as Trach Tube Kit has a component labeling discrepancy.
Summary by Recall Canary from the FDA notice
What happened
Medline Industries, LP, of Northfield, Illinois, began a recall on July 10, 2026, of its Medline medical convenience kit labeled as TRACH TUBE KIT, due to a component labeling discrepancy. The FDA added the recall to its Enforcement Report and classified it on August 21, 2026. The recall involves 45 kits distributed in California.
What to do
We don't have product-specific instructions for this recall. FDA's general advice for medical device recalls:
- A device recall doesn't always mean you must stop using it: it may need to be checked, adjusted or fixed.
- Talk to your health care provider before you stop using it.
Is yours affected?
Match the SKU, UDI-DI and lot code listed under your product.
A UDI-DI is the device identifier printed with the barcode on the device label.
Medline medical convenience kit labeled as: Trach Tube Kit
- SKU
- DYKM2330
- UDI-DI
- 10198459582158
- 40198459582159
- Lot code
- 26FLA408
Recall details
- Company began the recall
- Sold in
US Nationwide distribution in the state of California.
- Company
- Medline Industries, LPNorthfield, Illinois
- Hazard
- Labeling error
- Risk
Moderate risk
Using it may cause short-term health problems, or ones that treatment can reverse. Serious harm is unlikely.
FDA Class II recall · How risk is rated
- Event ID
- 99506
- Recall number
- Z-2999-2026
- Quantity recalled
- 45 kits
All recalls from Medline Industries, LP
Timeline
FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.
Company began the recall
Added to FDA's Enforcement Report · Classified by FDA
Listed on Recall Canary
In FDA's weekly enforcement report
Summary updated
