Medline recalls medical convenience kits labeled EYE TRAY-LF (SKU DYNJ21627P) due to incorrect syringes inside. The kits contain U-100 insulin syringes instead of the labeled 1mL Luer Lock Tuberculin syringes.
Specific Medline Kits contain Cardinal Health Monoject 1mL Luer Lock Syringes, Tuberculin Print, Sterile. Cardinal Health has recalled these syringes because the 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.
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Contact the company
📍Recalling firmMedline Industries, LP3 Lakes Dr · Northfield, IL 60093-2753
✎ GovInfoNow plain-language explainer
Medline is recalling medical convenience kits labeled EYE TRAY-LF (SKU DYNJ21627P) because they contain U-100 insulin syringes instead of the labeled 1mL Luer Lock Tuberculin syringes. This mix-up could lead to incorrect medication use if the syringes are used for injections. Read more at govinfonow.com/recall/49507-medline-eye-tray-lf-kit-recall-wrong-syringes-inside.
“Medline EYE TRAY-LF Kit Recall: Wrong Syringes Inside.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/49507-medline-eye-tray-lf-kit-recall-wrong-syringes-inside. Based on FDA recall #Z-2260-2026 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2260-2026%22&limit=1).
Medline Industries, LP recalled Medline medical convenience kits labeled as EYE TRAY-LF (SKU DYNJ21627P) due to containing mislabeled syringes, the FDA said on April 10, 2026. The hazard involves Cardinal Health Monoject syringes inside being U-100 insulin syringes rather than the labeled 1 mL Luer Lock Tuberculin Syringes.
How to tell if you have it
Brand: Medline
Product: Medline medical convenience kit labeled as EYE TRAY-LF, Medline Kit SKU DYNJ21627P
Lot Numbers: 26BMC538
Distribution: US Nationwide distribution in the states of California
The hazard
The recall affects specific Medline Kits containing Cardinal Health Monoject 1mL Luer Lock Syringes, Tuberculin Print, Sterile. Cardinal Health recalled these syringes because the 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.
Context
GovInfoNow's records show Medline Industries, LP has 68 other recalls on record since July 31, 2025. Other recent recalls of similar products include Medline Convenience Kits Recall: Fungal Contamination Risk (Aug. 11, 2026) and Medline Sinus Packs with Sharp Brush Edges Recalled for Cut Risk (Aug. 10, 2026). Other recent recalls of similar products include Cardinal Health Monoject Tuberculin Syringe Recall: Wrong Insulin Syringes in Packaging (Feb. 27, 2026), AVID Medical Halyard PERC TRAY Kit Recall: Risk of Syringe Disconnection (March 13, 2026), and Becton Dickinson 10mL Non-Sterile Luer-Lok Syringes Recalled Due to Wrong Syringe Type (Jan. 27, 2026).
How to tell if you have this one
Check for the EYE TRAY-LF label and SKU DYNJ21627P on the kit. Look for lot numbers 26BMC538 on the carton.
Brand
Medline
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Check Kit Contents
Verify if the kit contains U-100 insulin syringes instead of the labeled 1mL Luer Lock Tuberculin syringes.
Where it went and when
Where it was distributed
Distributed nationwide.
Nationwide
Not listed
FDA distribution: “US Nationwide distribution in the states of California.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA published this recall 54 days after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #Z-2260-2026 (April 10, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2260-2026 to see it in context.
Plain-language summary written by qwen3:4b on August 18, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.