LEADER brand Eye Irritation Relief (Polyvinyl alcohol 0.5%, Povidone 0.6%, Tetrahydrozoline Hydro...

FDA Recall #D-0131-2024 — Class I — October 31, 2023

Recall #D-0131-2024 Date: October 31, 2023 Classification: Class I Status: Ongoing

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.

Recalling Firm

Cardinal Health Inc. — Dublin, OH

Classification

Class I — Reasonable probability of serious adverse health consequences or death.

Product Type

Drugs

Product Quantity

11629 units

Distribution

Nationwide in the USA

Code Information

ALL LOTS

Status

Ongoing

Voluntary / Mandated

Voluntary: Firm initiated