FDA DrugsClass II
Vista Gel Hypromellose USP 0.3% w/v, Eye Drops Dry Eye Relief Lubricating Gel, 1...
Published: March 4, 2026Recall ID: D-0347-2026Category: drugsCountry: US
Reason for Recall / Hazard
Lack of Assurance of Sterility: Products have not been manufactured in conformance with current good manufacturing practices.
Product Description & Identification
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.
Additional Source Details
| Field | Value |
|---|---|
| City | Bhiwadi |
| State | N/A |
| Openfda › Unii | 1IVH67816N |
| Openfda › Route | OPHTHALMIC |
| Openfda › Spl id | 47e991f9-4722-d647-e063-6294a90a022b |
| Openfda › Brand name | VISTA HYPROMELLOSE DRY EYE RELIEF |
| Openfda › Spl set id | b2c4954c-ed53-778a-e053-2a95a90ae0d0 |
| Openfda › Package ndc | 77790-002-10 |
| Openfda › Product ndc | 77790-002 |
| Openfda › Generic name | HYPROMELLOSE |
| Openfda › Product type | HUMAN OTC DRUG |
| Openfda › Substance name | HYPROMELLOSE 2910 (50 MPA.S) |
| Openfda › Manufacturer name | Red Wedding LLC |
| Openfda › Application number | M018 |
| Openfda › Is original packager | true |
| Event id | 98253 |
| Address 1 | H - 881 |
| Address 2 | N/A |
| Code info | All lots |
| Postal code | N/A |
| Report date | 20260304 |
| Product type | Drugs |
| Product quantity | 17,280 cartons |
| Reason for recall | Lack of Assurance of Sterility: Products have not been manufactured in conformance with current good manufacturing practices. |
| Voluntary mandated | Voluntary: Firm initiated |
| Recall initiation date | 20251231 |
| Initial firm notification | Letter |
| Center classification date | 20260225 |
Overview
- Recalling FirmWizcure Pharmaa Private Limited
- StatusOngoing
- Risk LevelClass II
- DistributionDistributed Nationwide in the USA