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FDA recall 99481: MICRO LABS USA INC: Dorzolamide HCl and Timolol Maleate Ophthalmic Solution

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FDARecall 99481Medicines

What to do

The FDA record of this recall has no instruction for consumers. Compare the lot codes below with your product. If they match, do not use it, and follow the notice of the firm or ask the store where you bought it. Talk to your pharmacist or doctor before stopping a medicine.Note from Recalls Watch, not agency text.

Read the official notice on accessdata.fda.gov (opens in a new tab)

Hazard

Why it was recalled

Defective Container: Firm received multiple complaints of broken cap spikes and undeliverable drops.
Text from FDA, unedited.

FDA classification: Class II. Use may cause temporary or medically reversible health consequences, or the chance of serious consequences is remote. Status: Ongoing.

Is it yours? Products and codes

  • 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 or code
    Lot # DLHU0031, Exp Date: 06/30/2027.
    FDA recall number
    D-0730-2026

Distribution (FDA): Nationwide in the USA.

About this record

Issued by
U.S. Food and Drug Administration
Firm
MICRO LABS USA INC
Title
Composed by Recalls Watch from fields of the record; FDA records have no title.

If someone was hurt or swallowed something: call 911, or Poison Help at 1-800-222-1222.

About this recall

What is the hazard?

FDA states: “Defective Container: Firm received multiple complaints of broken cap spikes and undeliverable drops.”

What should I do if I have this product?

The FDA record of this recall has no instruction for consumers. Compare the lot codes on the notice with your product and follow the notice of the firm. The official report is linked on this page.

How do I know if my product is included?

Compare the lot or code printed on your product with the codes FDA lists on this notice, product by product.

When was this recall published?

FDA published recall 99481 on August 5, 2026.

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