FDA recall, , Moderate risk
Oasis Tears PF Preservative-Free Lubricant Eye Drops
Oasis Tears PF lubricant eye drops lack assurance of sterility.
Summary by Recall Canary from the FDA notice
What happened
Oasis Medical, Inc., of Glendora, California, recalled Oasis Tears PF, Preservative-Free Lubricant Eye Drops, 10mL/0.34 Fl OZ Bottle, Sterile, because of a lack of assurance of sterility. The recall began April 27, 2026, after FDA observations during an inspection of Excelvision. The product was distributed nationwide within the United States. The FDA added the recall to its Enforcement Report on May 8, 2026.
What to do
We don't have product-specific instructions for this recall. FDA's general advice for medicine recalls:
- Check the FDA or company notice for instructions specific to this product.
- Ask your pharmacist or doctor whether your lot is affected and what to do.
Is yours affected?
Match the NDC and lot code listed under your product.
An NDC (National Drug Code) is usually printed on the drug's label.
- NDC
- 42126-6400-1
- Lot code
- 1V59
- 3V12
- 3V69
Recall details
- Company began the recall
- Sold in
Nationwide within the United States
- Company
- Oasis Medical, Inc.Glendora, California
- Hazard
- Sterility problem
- Risk
Moderate risk
Taking it may cause short-term health problems, or ones that treatment can reverse. Serious harm is unlikely.
FDA Class II recall · How risk is rated
- Event ID
- 98897
- Recall number
- D-0525-2026
Timeline
FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.
Company began the recall
Added to FDA's Enforcement Report · Classified by FDA
Listed on Recall Canary
In FDA's weekly enforcement report
Summary updated
