FDA-Drug2026-03-04Class IIPROCESSING DEFECT
Vista Gel Hypromellose eye drops recalled for sterility concerns
What this means
Vista Gel Hypromellose eye drops were not manufactured according to FDA safety standards, which means the product may not be sterile. The eye drops were distributed nationwide in the United States. No injuries have been reported.
- Stop using Vista Gel Hypromellose eye drops immediately
- Do not put the product in your eyes
- Contact hi-health or your pharmacy for a refund or replacement
- Talk to your doctor about safe alternative eye drops for dry eye relief
The agency's original wording
Hazard
Lack of Assurance of Sterility: Products have not been manufactured in conformance with current good manufacturing practices.
Intended for
All ages
Illnesses reported
None reported
Sold states
Distributed Nationwide in the USA
Affected count
17,280 cartons
Manufactured in
H - 881, N/A, Bhiwadi, N/A, India
Products
Vista Gel Hypromellose USP 0.3% w/v, Eye Drops Dry Eye Relief Lubricating Gel, 10 ml. (1/3 fl. oz), Wizcure Pharmaa PVT. LTD, H-881, Phase-3, RIICO Industrial Area, Bhiwadi-301019, India, Manufactured for and distributed by: hi-health, 15207 N. 75th Street, Suite #104, Scottsdale, AZ, 85260, NDC 77790-002-10.
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0347-2026Want us to check the next one for you?
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