CLASS II ONGOING Drug recall · Reported 6 Aug 2025 · FDA Enforcement Report

Timolol Maleate Ophthalmic Solution USP, 0.5%, Sterile recalled by FDC

FDC is recalling Timolol Maleate Ophthalmic Solution USP, 0.5%, Sterile, distributed nationwide in the US. The recall was initiated on 5 Jul 2025 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot#: 083L061, Exp.: 11/2025.
NDC64980-513, 64980-514
UPC0364980513050
Quantity recalled154,176 bottles

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

Recall details

Recall number
D-0543-2025
FDA event ID
97219
Recalling firm
FDC, Aurangabad, Maharashtra State
Manufacturer
Rising Pharma Holdings, Inc.
Classification
Class II
Status
Ongoing
Recall initiated
5 Jul 2025
FDA classified
29 Jul 2025
Reported
6 Aug 2025
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Other Reasons
Drug class
Eye Drops

Timeline

5 Jul 2025Recall initiated by company
29 Jul 2025Classified by FDA+24 days
6 Aug 2025Published in enforcement report+8 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Defective Container: spike of the cap becomes lodged in the nozzle of the product bottle.

Product as listed by the FDA

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.

Where it was distributed

U.S Nationwide.

Nationwide

Questions about this recall

Why was it recalled?

Defective Container: spike of the cap becomes lodged in the nozzle of the product bottle.

Which lots are affected?

Lot#: 083L061, Exp.: 11/2025.

Where was it sold?

U.S Nationwide.

What should I do if I have it?

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

More recalls from FDC

All 11
ReportedClassRecallCompanyReasonWhere
DrugCLASS IITimolol Maleate Ophthalmic Solution USP, 0.5%, Sterile recalled by FDCTimolol MaleateFDCOtherNationwide
DrugCLASS IICiprofloxacin Ophthalmic Solution USP, 0.3% as base, package recalledCiprofloxacinFDCPackaging DefectsNationwide
DrugCLASS IITimolol Maleate Ophthalmic Solution USP, 0.5%, Sterile recalled by FDCTimolol MaleateFDCOtherNJ
DrugCLASS IICiprofloxacin Ophthalmic Solution USP, 0.3% as base recalled by FDCCiprofloxacinFDCPackaging DefectsNationwide
DrugCLASS IITimolol Maleate Ophthalmic Solution USP, 0.25%, Sterile recalled by FDCTimolol MaleateFDCOtherNJ

Other Timolol recalls

All 20
ReportedClassRecallCompanyReasonWhere
DrugCLASS IITimolol Maleate Ophthalmic Solution USP, 0.5%, Sterile recalled by FDCTimolol MaleateFDCOtherNationwide
DrugCLASS IITimolol Maleate Ophthalmic Solution USP, 0.5%, Sterile recalled by FDCTimolol MaleateFDCOtherNJ
DrugCLASS IITimolol Maleate Ophthalmic Solution USP, 0.25%, Sterile recalled by FDCTimolol MaleateFDCOtherNJ
DrugCLASS IITimolol Maleate Ophthalmic Solution USP, 0.5%, Sterile recalled by FDCTimolol MaleateFDCOtherNJ
DrugCLASS IITimolol Maleate Ophthalmic Solution recalled by FDCTimolol MaleateFDCPackaging DefectsNationwide