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.
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.
The kits contain U-100 insulin syringes instead of the labeled 1mL Luer Lock Tuberculin syringes. Using insulin syringes for non-insulin injections could cause incorrect dosing or injury.
Healthcare workers and patients using Medline EYE TRAY-LF kits (SKU DYNJ21627P) with specific lot numbers. Those using insulin syringes for non-insulin purposes may be at risk.
Check for the EYE TRAY-LF label and SKU DYNJ21627P on the kit. Look for lot numbers 26BMC538 on the carton.
Verify if the kit contains U-100 insulin syringes instead of the labeled 1mL Luer Lock Tuberculin syringes.
The kits contain U-100 insulin syringes instead of the labeled 1mL Luer Lock Tuberculin syringes, which could lead to incorrect medication use.
Check if the kit contains U-100 insulin syringes. If so, stop using it and contact Medline for guidance.
Look for the EYE TRAY-LF label and SKU DYNJ21627P with lot number 26BMC538 on the carton.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2260-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2260-2026 from Medline. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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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.
