Class II · Moderate risk Ongoing
Rohto Cooling Eye Drops Digi Eye
Reason Lack of Assurance of Sterility
ImproVue Ophthalmic Lubricant Drops
Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.
Why it was recalled
Failed pH specification
What was recalled
ImproVue Ophthalmic Lubricant Drops (1.7% Hypromellose), 1 Single Use Syringe, 0.07 fl oz (2mL), 1 Single Use Applicator Tip per carton, Manufactured for OCULUS SURGICAL, Port St. Lucie, FL 34986, NDC 62144-5510-05
- Recalling firm
- Oasis Medical, Inc.
- NDC code
- 62144-5510-05
- Origin
- CA, United States
- Initiated by
- Voluntary: Firm initiated
- FDA recall number
- D-1084-2015
What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.
Other Hypromellose recalls
See all
Class II · Moderate risk Ongoing
Rohto Cooling Eye Drops ALL-IN-ONE
Reason Lack of Assurance of Sterility
Class II · Moderate risk Ongoing
Artificial Tears Lubricant Eye Drops
Reason Lack of Assurance of Sterility
Class II · Moderate risk Ongoing
Dry Eye Relief Eye Drops
Reason Lack of Assurance of Sterility
Class II · Moderate risk Ongoing
Vista Gonio Eye Lubricant
Reason Lack of Assurance of Sterility: Products have not been manufactured in conformance with current good manufacturing practices.
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