Recalls / Class II
Class IID-0347-2026
Product
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.
- Brand name
- Vista Hypromellose Dry Eye Relief
- Generic name
- Hypromellose
- Active ingredient
- Hypromellose 2910 (50 Mpa.s)
- Route
- Ophthalmic
- NDC
- 77790-002
- FDA application
- M018
- Affected lot / code info
- All lots
Why it was recalled
Lack of Assurance of Sterility: Products have not been manufactured in conformance with current good manufacturing practices.
Recalling firm
- Firm
- Wizcure Pharmaa Private Limited
- Manufacturer
- Red Wedding LLC
- Notification channel
- Letter
- Type
- Voluntary: Firm initiated
- Address
- H - 881, N/A, Bhiwadi, N/A N/A, India
Distribution
- Quantity
- 17,280 cartons
- Distribution pattern
- Distributed Nationwide in the USA
Timeline
- Recall initiated
- 2025-12-31
- FDA classified
- 2026-02-25
- Posted by FDA
- 2026-03-04
- Status
- Ongoing
Source: openFDA Drug Enforcement endpoint. Recall record D-0347-2026. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.