FDA recall, , Moderate risk
Optase Dry Eye Intense Drops (Glycerin 0.2%)
Optase Dry Eye Intense Drops lack assurance of sterility.
Summary by Recall Canary from the FDA notice
What happened
SCOPE HEALTH, of New York, New York, recalled Optase Dry Eye Intense Drops (Glycerin 0.2%), packaged in 0.33 fl oz, Sterile, manufactured for Scope Health Inc., due to a lack of assurance of sterility. The recall began April 20, 2026, and the product was distributed nationwide within the United States.
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.
Optase Dry Eye Intense Drops (Glycerin 0.2%)
- NDC
- 72972-002-01
- Lot code
- 8T98
- 9T31
- 9T32
- 2V13
- 2V14
- 2V15
- 3V35
- 3V36
- 3V37
- 5V45
- 5V46
- 9V12
- 1X57
- 1X70
- 1X84
Recall details
- Company began the recall
- Sold in
Nationwide within the United States
- Company
- SCOPE HEALTHNew York, New York
- 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
- 98802
- Recall number
- D-0499-2026
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
