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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 96014

1 recalled-product record grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
December 16, 2024
Product types
Drug
Classifications
Class II
Statuses
Ongoing
Recalling firm wording
FDC Limited

Dossier provenance

Source snapshots represented here

  • openFDA Drug Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

1 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

drug · product 1 of 1

Ciprofloxacin Ophthalmic Solution USP, 0.3% as base, Sterile, package in 5 mL bottles, Rx Only, Distributed by: Leading Pharma LLC, Fairfield, NJ. Manufactured by: FDC Limited, Maharashtra, India, NDC 69315-308-05

D-0182-2025
Recall number
D-0182-2025
Initiated
December 16, 2024
Classification
Class II
Status
Ongoing
Recalling firm
FDC Limited
Quantity
136,181 bottles

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Defective container: Unable to get the solution out of the bottle as the spike of the cap was lodged in the nozzle of the product bottle

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Defective container: Unable to get the solution out of the bottle as the spike of the cap was lodged in the nozzle of the product bottle

Code information

Lot: 083L111, Exp. 11/30/2025; 084A032, Exp. 12/31/2025

Distribution pattern

Nationwide