FDA recall record

Timolol Maleate Ophthalmic Solution USP, 0.5%, Sterile, 5mL bottles recall — FDA D-0632-2024

Defective container; yellow colored spike from cap lodged in the nozzle

Class IIclassification
D-0632-2024official record ID
Aug 21, 2024report date

Recall record at a glance

Official recordD-0632-2024
CategoryDrug Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmFDC Limited
Report dateAug 21, 2024
Recall initiation dateJul 18, 2024
Quantity362,544 bottles
LocationAurangabad, Maharashtra State, India

Official product description

Timolol Maleate Ophthalmic Solution USP, 0.5%, Sterile, 5mL bottles, Rx only, Manufactured by: FDC Limited, Waluj, Aurangabad, Maharashtra, India, Distributed by: Rising Pharmaceuticals Inc, New Jersey, [NDC 64980-514-05].

Why the product was recalled

Defective container; yellow colored spike from cap lodged in the nozzle

Distribution information

Nationwide in the US

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

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

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