FDA recall, , Moderate risk
Medline Eye Tray-LF Medical Convenience Kit
The Medline Eye Tray-LF kit contains syringes labeled as 1 mL but are U-100 insulin syringes.
Summary by Recall Canary from the FDA notice
What happened
Medline Industries, LP, of Northfield, Illinois, recalled 8 Medline medical convenience kits labeled as EYE TRAY-LF because the kits contain Cardinal Health Monoject 1mL Luer Lock Syringes, Tuberculin Print, Sterile, which Cardinal Health recalled. The syringes' outer carton and blister pack are labeled as a 1 mL Luer Lock Tuberculin Syringe (Product Code 1180100777), but the syringes inside are U-100 insulin syringes.
The recall began April 10, 2026, and was added to the FDA's Enforcement Report on May 28, 2026. The kits were 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 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 medical convenience kit labeled as Eye Tray-LF
- SKU
- DYNJ21627P
- UDI-DI
- 10198459151569
- 40198459151560
- Lot code
- 26BMC538
Recall details
- Company began the recall
- Sold in
US Nationwide distribution in the states 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
- 98866
- Recall number
- Z-2260-2026
- Quantity recalled
- 8 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
