FDA recall record

LUBRICANT DROPS Leader brand Lubricant Eye Drops recall — FDA D-0291-2024

Non-Sterility

Class Iclassification
D-0291-2024official record ID
Feb 14, 2024report date

Recall record at a glance

Official recordD-0291-2024
CategoryDrug Recalls
ClassificationClass I
FDA record statusOngoing
Recalling firmKilitch Healthcare India Limited
Report dateFeb 14, 2024
Recall initiation dateNov 13, 2023
Quantity210,192 bottles
LocationNavi Mumbai, India

Official product description

Leader brand Lubricant Eye Drops (Carboxymethylcellulose Sodium 0.5%), packaged in a) 0.5 FL OZ (15mL) bottles (Single Pack) (NDC 70000-0090-1) and b) 0.5 FL OZ (15 mL) bottles (Twin pack) (NDC 70000-0090-2), Distributed by: Cardinal Health Dublin, Ohio 43017

Why the product was recalled

Non-Sterility

Distribution information

Nationwide within the United States

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Press Release.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.

Related recall records

Other records from the same recalling company are shown first when available.