Dorzolamide HCl and Timolol Maleate Ophthalmic Solution,… was recalled on July 22, 2026 in cooperation with the U.S. Food and Drug Administration because defective Container: Firm received multiple complaints of broken cap spikes and undeliverable drops..
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.
Lot # DLHU0031, Exp Date: 06/30/2027.
Units affected: N/A
Where it was sold: Nationwide in the USA.
Compare the codes above against the label on your product — usually on the bottom, the back panel, or the packaging. If your unit isn't listed, it is not part of this recall.
Defective Container: Firm received multiple complaints of broken cap spikes and undeliverable drops.
Class II means the product might cause a temporary or medically reversible health problem; the chance of serious harm is remote.
Stop using the product. Return it to the place of purchase for a refund, or dispose of it. Contact the recalling firm with questions.
Contact: Recalling firm: MICRO LABS USA INC
Not sure what you're entitled to? Read our guide: what to do if your product is recalled.
Always confirm details on the official notice from the U.S. Food and Drug Administration before acting.
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Failed Content Uniformity Specifications
Failed Impurities/Degradation Specifications
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