HIGH

Wizcure Pharmaa Recalls Eye Drops Due to Sterility Concerns

Wizcure Pharmaa recalled 5,760 cartons of Vista Tears Eye Drops on December 31, 2025. The recall follows a lack of assurance of sterility in the product. Consumers should stop using the drops immediately and contact a healthcare provider for guidance.

Quick Facts at a Glance

Recall Date
December 31, 2025
Hazard Level
HIGH
Brand
Wizcure Pharmaa
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

Get instant alerts for Health & Personal Care recalls

Be the first to know. Free instant alerts to your inbox.

No spamUnsubscribe anytime

Product Details

The recalled product is Vista Tears Polyethylene Glycol 400 0.4% w/v and Propylene Glycol 0.3% w/v Eye Drops. The product is packaged in 10 ml (1/3 fl. oz.) bottles. It was manufactured by Omni Lens Pvt. Ltd. and distributed by hi-health.

The Hazard

The eye drops lack assurance of sterility due to non-compliance with good manufacturing practices. This poses a potential risk of eye infections or other serious health issues.

Reported Incidents

No specific incidents or injuries related to the product have been reported as of the recall date. However, the risk of infection remains a serious concern.

What to Do

Stop using the Vista Tears Eye Drops immediately. Contact Wizcure Pharmaa or your healthcare provider for further guidance. Consumers may also return the product for a refund.

Contact Information

For more information, contact Wizcure Pharmaa at their distribution center in Scottsdale, AZ. Visit the FDA recall notice at https://www.accessdata.fda.gov/scripts/enforcement/enforce_rpt-Product-Tabs.cfm?recall_number=D-0346-2026.

Key Facts

  • 5,760 cartons recalled nationwide
  • Lack of sterility assurance
  • Distributed by hi-health in Scottsdale, AZ
  • Contact healthcare provider for guidance

Get Alerts for Health & Personal Care Recalls

Get instant alerts for recalls that affect you. Free forever.

Safety Assessment

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

Product Details

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

Related Recalls

HIGH

AvKARE Recalls Amantadine HCl Capsules Over Dissolution Issues

AvKARE recalled Amantadine HCl capsules on February 13, 2026, due to failed dissolution specifications. The recall affects the 100 mg capsules, which may not dissolve properly. Consumers should stop using this product and contact their healthcare provider immediately.

AMANTADINE HCL
Failed Dissolution
Read more
HIGH

Eptifibatide Injection Recalled Over Labeling Error

Slate Run Pharmaceuticals recalled Eptifibatide Injection on February 12, 2026. The recall affects all lots of the 75 mg/100 mL vial due to incorrect dosing information. Healthcare providers and consumers must stop using the product immediately.

Eptifibatide
Labeling: Not
Read more
HIGH

LEO Pharma Recalls Adbry Injection Over Sterility Concerns

LEO Pharma Inc. recalled 11,407 units of Adbry injection on February 10, 2026. The recall stems from a lack of assurance of sterility due to particulate matter identified as wool fiber. Consumers should stop using the product immediately and contact their healthcare provider for guidance.

ADBRY
Lack of
Read more
HIGH

Hitachi Proton Beam Therapy System Recalled Due to Software Issue

Hitachi recalled its Proton Beam Therapy System on February 6, 2026, due to a software anomaly that may result in positional discrepancies. The recall affects one unit distributed in Texas and Washington D.C. Healthcare providers and patients must stop using the device immediately.

Hitachi
Software anomaly
Read more
HIGH

Fresenius Kabi Vancomycin Injection Recalled Over Sterility Concerns

Fresenius Kabi Compounding recalled its vancomycin HCl injection on February 5, 2026, due to a lack of assurance of sterility. This Class II recall affects all lots distributed nationwide. Healthcare providers and consumers must stop using the product immediately.

Fresenius Kabi Compounding
Lack of
Read more