Are My Eye Drops Safe?

A search tool from the Dry Eye Foundation

Alerts
FDA Action Title
No Known Current Alerts
Active Recall
Country of Manufacture
Most recent FDA communication
Active Recall
FDA Public Warning
FDA Warning Letter
Frankenstein Eye Drop
Discontinued
Generic
Generic for:
Refresh Plus Eye Drops
Active Recall
FDA Public Warning
FDA Warning Letter
Possible Frankenstein Eye Drop
Discontinued
Generic
Generic for:
Refresh Plus Eye Drops
Active Recall
FDA Public Warning
FDA Warning Letter
Discontinued
Generic
Generic for:
Lubrifresh
FDA Warning Letter
Frankenstein Eye Drop
Non-Compliant Ingredients
Prescription Drug Claims
Not Registered with FDA
FDA Warning Letter
Frankenstein Eye Drop
Non-Compliant Ingredients
Prescription Drug Claims
Not Registered with FDA
FDA Public Warning
FDA Warning Letter
Frankenstein Eye Drop
Non-Compliant Ingredients
Prescription Drug Claims
Not Registered with FDA
FDA Warning Letter
Frankenstein Eye Drop
Non-Compliant Ingredients
Prescription Drug Claims
Not Registered with FDA
FDA Warning Letter
Frankenstein Eye Drop
Non-Compliant Ingredients
Not Registered with FDA
FDA Warning Letter
Frankenstein Eye Drop
Non-Compliant Ingredients
Prescription Drug Claims
Not Registered with FDA
FDA Warning Letter
Frankenstein Eye Drop
Non-Compliant Ingredients
Prescription Drug Claims
Not Registered with FDA
FDA Warning Letter
Frankenstein Eye Drop
Non-Compliant Ingredients
Prescription Drug Claims
Not Registered with FDA
FDA Warning Letter
Frankenstein Eye Drop
Non-Compliant Ingredients
Prescription Drug Claims
Not Registered with FDA
FDA Warning Letter
Frankenstein Eye Drop
Non-Compliant Ingredients
Prescription Drug Claims
Not Registered with FDA
FDA Warning Letter
Frankenstein Eye Drop
Non-Compliant Ingredients
Prescription Drug Claims
Not Registered with FDA
FDA Warning Letter
Frankenstein Eye Drop
Non-Compliant Ingredients
Prescription Drug Claims
Not Registered with FDA
Active Recall
Manufacturing Violations
Generic
Generic for:
Stye Sterile Lubricant Eye Ointment
Active Recall
Manufacturing Violations
Generic
Generic for:
Refresh P.M.
Active Recall
FDA Public Warning
Manufacturing Violations
Generic
Generic for:
Stye Sterile Lubricant Eye Ointment
Active Recall
FDA Public Warning
Manufacturing Violations
Generic
Generic for:
Refresh P.M.
Visibly Adulterated
Visibly Adulterated

Learn more about these flags
Feb 2-5, DEF verified 8 different packages of Freshkote single use vials with visible solid matter in the vials. The manufacturer has opened an investigation.

FDA Public Warning
Possible Frankenstein Eye Drop
Non-Compliant Ingredients
Prescription Drug Claims
Not Registered with FDA
FDA Public Warning
Possible Frankenstein Eye Drop
Non-Compliant Ingredients
Prescription Drug Claims
Not Registered with FDA
FDA Public Warning
Possible Frankenstein Eye Drop
Non-Compliant Ingredients
Prescription Drug Claims
Not Registered with FDA
FDA Public Warning
Manufacturing Violations
Generic
Generic for:
Systane Lubricant Eye Gel
FDA Public Warning
Manufacturing Violations
Generic
Generic for:
Systane Complete