Medline recalls procedure kits labeled OL OCULAR with leaking sterile water and saline bottles. Affected kits may cause contamination if used improperly. Contact Medline for replacement.
It was identified that the Medline Sterile Water and Medline Sterile 0.9% Normal Saline bottles were leaking at the interface of the peel-foil and bottle opening.
Medline is recalling procedure kits labeled 'OL OCULAR' because the sterile water and saline bottles leak at the bottle opening. This could lead to contamination of medical procedures if the kits are used without the leaks being fixed.
The bottles leak at the interface where the peel-foil meets the bottle opening. This leak could allow contaminants to enter the sterile solution, potentially causing infections during medical procedures.
Healthcare professionals using Medline procedure kits labeled 'OL OCULAR' are most at risk. Patients receiving procedures with these kits could face contamination if the leaks are not addressed.
Check for kits labeled 'OL OCULAR' with reference number DYNJ906183K. Lot numbers 23LME299 are affected. These kits were sold with UDI/DI numbers 10195327385521 (EA) and 10195327385522 (CS).
Inspect the bottles for leaks at the interface of the peel-foil and bottle opening.
Reach out to Medline for replacement kits if leaks are found.
The kits may have leaking bottles, which could cause contamination. Do not use if leaks are present.
Look for kits labeled 'OL OCULAR' with reference number DYNJ906183K and lot number 23LME299.
Contact Medline for replacement kits to ensure safe use.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1713-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-1713-2025 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.
