Scope Health: Optase Dry Eye Intense Drops (glycerin 0.2%)

Recall Summary Scope Health is recalling Optase Dry Eye Intense Drops (Glycerin 0.2%) in 0.33 fl oz bottles nationwide because the manufacturer cannot confirm the product is sterile. The affected product has NDC number 72972-002-01 and was distributed across all U.S. states and Washington, DC. This is a Class II recall, meaning use of the product could cause serious health problems or death.

Recalling firm
SCOPE HEALTH
Product
Optase Dry Eye Intense Drops (Glycerin 0.2%), packaged in 0.33 fl oz, Sterile, Manufactured for Scope Health Inc., 79 Madison Ave., 8th Floor, New York, NY 10016, USA, NDC 72972-002-01.
Reason
Lack of Assurance of Sterility
Classification
Class II
Category
drug recall
Country
United States
Agency
U.S. Food and Drug Administration
Recall date
2026-04-20
Status
Ongoing
Areas affected
AL, AK, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, ...
Distribution
Nationwide within the United States

Official recall notice from U.S. Food and Drug Administration

Recall details on Nibble Recalls: https://trynibble.app/recalls/fb6c11d1-5ce8-4340-8a23-fc01ad69e48e