FDA recall, , Moderate risk
Medline Foot Ankle Convenience Kit
The Medline convenience kit labeled Foot Ankle has a discrepancy in the shelf-life of a component.
Summary by Recall Canary from the FDA notice
What happened
Medline Industries, LP recalled its Medline convenience kit labeled FOOT ANKLE because of a discrepancy in the shelf-life of a component. The company began the recall on September 11, 2026, and the FDA added it to its Enforcement Report on October 15, 2026, with the same classification date. The recall involves 30 kits with distribution in New York.
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 your kit 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 convenience kit labeled as: Foot Ankle
- SKU
- DYNJ65395A
- UDI-DI
- 10195327174156
- 40195327174157
- Lot code
- 22GBW912
Recall details
- Company began the recall
- Sold in
US Nationwide distribution in the state of New York.
- Company
- Medline Industries, LP
- Hazard
- Device defect
- 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
- 99983
- Recall number
- Z-0189-2027
- Quantity recalled
- 30 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
