Oasis Tears PF Eye Drops Recall: Lack of Sterility Assurance
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.
Lower-risk recall
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.
Contact the company
What happened, in plain English
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. Read more at govinfonow.com/recall/31328-oasis-tears-pf-eye-drops-recall-lack-of-sterility-assurance.
Source Summary by GovInfoNow · govinfonow.com/recall/31328-oasis-tears-pf-eye-drops-recall-lack-of-sterility-assurance · Updated August 17, 2026 · FDA enforcement record: FDA #D-0525-2026
Cite this page
“Oasis Tears PF Eye Drops Recall: Lack of Sterility Assurance.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/31328-oasis-tears-pf-eye-drops-recall-lack-of-sterility-assurance. Based on FDA recall #D-0525-2026 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0525-2026%22&limit=1).
Why it’s dangerous
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.
Who’s affected
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.
How to tell if you have this one
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.
- Brand
Oasis Medical- Category
Drug
What to do — step by step
Check Product Details
Identify the lot number and expiration date on the bottle to confirm if it's affected.
Where it went and when
Where it was distributed
Distributed nationwide.
FDA distribution: “Nationwide within the United States” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA published this recall 23 days after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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Where this comes from
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 #D-0525-2026 (April 27, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0525-2026 to see it in context.
- Plain-language summary written by qwen3:4b on August 17, 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.