Oasis Medical recalls preservative-free lubricant eye drops due to potential lack of sterility. Affected lots manufactured for OASIS in France with specific expiration dates.
Lack of Assurance of Sterility: The recall is being initiated out of an abundance of caution following FDA observations noted during a recent inspection of Excelvision.
Oasis Medical is recalling preservative-free lubricant eye drops because of a potential lack of sterility. This could pose a risk of infection if the product is used without proper sterility assurance.
The recall is initiated due to FDA observations during an inspection of Excelvision. The lack of sterility assurance means the product could cause infections if used without proper sterility.
People who own or use Oasis Tears PF eye drops with the specific lot numbers and expiration dates listed in the recall notice are affected. Those with the product in their possession are most at risk.
Check for the product name 'Oasis Tears PF, Preservative-Free Lubricant Eye Drops, 10mL/0.34 Fl OZ Bottle, Sterile'. Look for lot numbers 1V59, 3V12, or 3V69 with expiration dates of 05/31/26 or 08/31/26.
Identify the lot number and expiration date on the bottle to confirm if it's affected.
Oasis Tears PF, Preservative-Free Lubricant Eye Drops, 10mL/0.34 Fl OZ Bottle, Sterile, with lot numbers 1V59, 3V12, or 3V69 and expiration dates of 05/31/26 or 08/31/26.
The recall is initiated out of an abundance of caution following FDA observations noted during a recent inspection of Excelvision.
Check the lot number and expiration date on the bottle. If it matches the affected lots, contact Oasis Medical for further instructions.
We’ve drafted a message you can send Oasis Medical to request your refund or repair — edit it as you like.
Subject: Recall D-0525-2026 — Oasis Medical Oasis Medical Hello, I own a Oasis Medical that is covered by recall D-0525-2026 from Oasis Medical. 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.
