LEADER brand Eye Irritation Relief (Polyvinyl alcohol 0.5%, Povidone 0.6%, Tetrahydrozoline Hydrochloride 0.05%), 0.5 FL OZ (15 mL) dropper bottles, Sterile, Distributed By Cardinal Health, Dublin, Ohio 43017, Made in India NDC: 70000-0087-1
Reported: November 29, 2023 Initiated: October 31, 2023 #D-0131-2024
Product Description
LEADER brand Eye Irritation Relief (Polyvinyl alcohol 0.5%, Povidone 0.6%, Tetrahydrozoline Hydrochloride 0.05%), 0.5 FL OZ (15 mL) dropper bottles, Sterile, Distributed By Cardinal Health, Dublin, Ohio 43017, Made in India NDC: 70000-0087-1
Reason for Recall
Non-Sterility: FDA found insanitary conditions and positive bacterial test results from environmental sampling at the manufacturing facility.
Details
- Recalling Firm
- Cardinal Health Inc.
- Units Affected
- 11629 units
- Distribution
- Nationwide in the USA
- Location
- Dublin, OH
Frequently Asked Questions
What product was recalled? ▼
LEADER brand Eye Irritation Relief (Polyvinyl alcohol 0.5%, Povidone 0.6%, Tetrahydrozoline Hydrochloride 0.05%), 0.5 FL OZ (15 mL) dropper bottles, Sterile, Distributed By Cardinal Health, Dublin, Ohio 43017, Made in India NDC: 70000-0087-1. Recalled by Cardinal Health Inc.. Units affected: 11629 units.
Why was this product recalled? ▼
Non-Sterility: FDA found insanitary conditions and positive bacterial test results from environmental sampling at the manufacturing facility.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on November 29, 2023. Severity: Critical. Recall number: D-0131-2024.
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