HIGH

Wizcure Pharmaa Recalls Eye Drops Due to Sterility Risk

Wizcure Pharmaa PVT. LTD. recalled 11,520 cartons of Vista Meibo Tears Eye Drops on December 31, 2025. The recall occurred due to lack of assurance of sterility, posing a high risk to consumers. The affected product was distributed nationwide in the USA.

Quick Facts at a Glance

Recall Date
December 31, 2025
Hazard Level
HIGH
Brands
Wizcure Pharmaa, Vista Meibo Tears
Category
Health & Personal Care
Sold At
Multiple Retailers
Geographic Scope
1 states
At-Risk Groups
GENERAL

Hazard Information

Lack of Assurance of Sterility: Products have not been manufactured in conformance with current good manufacturing practices.

What You Should Do

Consumers and healthcare providers should stop using this product immediately. Contact Wizcure Pharmaa Private Limited or your healthcare provider for guidance. Notification method: Letter

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Product Details

The recalled product is Vista Meibo Tears Propylene Glycol 0.6% w/v Eye Drops, 10 ml. It was manufactured by Wizcure Pharmaa PVT. LTD. and distributed by hi-health. The product was available in various retail outlets across the USA.

The Hazard

The eye drops lack assurance of sterility. This defect can lead to serious eye infections or complications.

Reported Incidents

No specific incidents or injuries have been reported in connection with this recall as of now. However, the potential risk due to lack of sterility could affect users.

What to Do

Consumers should stop using the affected eye drops immediately. Contact Wizcure Pharmaa for further guidance and follow the notification method provided.

Contact Information

For more information, consumers can reach Wizcure Pharmaa at their official website or through their customer service.

Key Facts

  • Recalled product: Vista Meibo Tears Eye Drops
  • Quantity: 11,520 cartons
  • Recall date: December 31, 2025
  • Hazard: Lack of assurance of sterility
  • Distribution: Nationwide in the USA

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Safety Assessment

Risk LevelHIGH
Severity Score
8/ 10
Affected Groups
GENERAL
Injury Types
OTHER

Product Classification

Product Details

Model Numbers
All lots
UPC Codes
77790-003
77790-003-10
Affected States
ALL
Report Date
March 4, 2026
Source Agency
FDA - Drug Safety
Recall Status
ACTIVE

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