FDA recall record

Dorzolamide HCl and Timolol Maleate Ophthalmic Solution, USP, 2%/0.5%, 10mL - bottle recall — FDA D-0730-2026

Defective Container: Firm received multiple complaints of broken cap spikes and undeliverable drops.

Class IIclassification
D-0730-2026official record ID
Aug 5, 2026report date

Recall record at a glance

Official recordD-0730-2026
CategoryDrug Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmMICRO LABS USA INC
Report dateAug 5, 2026
Recall initiation dateJul 22, 2026
QuantityN/A
LocationSomerset, NJ, United States

Official product description

Dorzolamide HCl and Timolol Maleate Ophthalmic Solution, USP, 2%/0.5%, 10mL - bottle, Rx only, Manufactured by: Micro Labs Limited, India, Manufactured for: Micro Labs USA Inc., Somerset, NJ 08873. NDC 42571-147-26.

Why the product was recalled

Defective Container: Firm received multiple complaints of broken cap spikes and undeliverable drops.

Distribution information

Nationwide in the USA.

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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