Wizcure Pharmaa Recalls Vista Tears Eye Drops Nationwide Over Sterility Concerns
Wizcure Pharmaa Private Limited is recalling all lots of Vista Tears Eye Drops due to a lack of sterility assurance and manufacturing practice violations.
What Happened
Wizcure Pharmaa Private Limited has initiated a voluntary recall of Vista Tears Eye Drops. The recall was issued due to a lack of assurance of sterility, as the products were not manufactured in conformance with current good manufacturing practices (cGMP). The recall is currently classified as a Class II event by the FDA.
Which Products Are Affected
The recall involves Vista Tears Polyethylene Glycol 400 0.4% w/v, Propylene Glycol 0.3% w/v Eye Drops, used for dry eye relief.
- Product Name: Vista Tears Lubricant Eye Drops
- Size: 10 ml (1/3 fl. oz.) sterile bottles
- NDC Number: 77790-001-10
- Affected Lots: All lots
- Quantity: 5,760 cartons
- Distribution: Distributed nationwide across the United States
- Manufacturer: Omni Lens Pvt. Ltd. (India) for hi-health (Scottsdale, AZ)
What You Should Do
Consumers should immediately stop using the affected Vista Tears Eye Drops. The recall was initiated via letter to distributors and retailers. Consumers who possess these products should contact their point of purchase or the distributor, hi-health, for further instructions regarding the return or disposal of the product.
Why This Matters
Products intended for use in the eyes must be sterile; a lack of sterility assurance poses a risk of eye infections or other health complications for users. This recall ensures that potentially contaminated products are removed from the market to protect consumer safety.
Source
Information provided by the FDA. Recall Number: D-0346-2026.
Source: FDA Official Notice