Elevated site urgencyFDA Class II

Dorzolamide HCl and Timolol Maleate Ophthalmic Solution, USP, 2%/0

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

Agency
FDA Drug
Recall date
Jul 22, 2026
Status
Ongoing
Company
MICRO LABS USA INC

1. What product was recalled?

Dorzolamide HCl and Timolol Maleate Ophthalmic Solution, USP, 2%/0

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.

Quantity: N/A

Code or lot text: Lot # DLHU0031, Exp Date: 06/30/2027.

LOT
Exp Date: 06/30/2027.
LOT
Lot # DLHU0031
NDC
42571-147
NDC
42571-147-26
RECALL-NUMBER
D-0730-2026
UPC
0342571147266

2. Is my exact product affected?

Compare every printed identifier. A matching value can indicate that your product is included.

3. What is the hazard?

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

4. What should I do now?

Follow the FDA recall notice and contact the recalling company for current instructions.

5. Where was it sold or distributed?

Nationwide

6. Were injuries or illnesses reported?

No separate injury or illness statement was present in the normalized record. Check the official source for the latest report.

7. What remedy is available?

Follow the FDA recall notice and contact the recalling company for current instructions.

8. Is the recall active or closed?

The source status is Ongoing. Recall Index urgency is elevated, which is a separate deterministic site label.

9. When was the information checked?

Last checked .

  1. unchanged
  2. created

10. Where is the official source?

Open the official FDA Drug source

Recall Index normalizes public source data for easier checking. Source agencies remain authoritative. Confirm identifiers and instructions at the official source.