Product Safety Recalls

Product Recall Tracker

CIPROFLOXACIN HYDROCHLORIDE Recall D-0182-2025

Description: 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

CIPROFLOXACIN HYDROCHLORIDE Recall D-0182-2025 Information

StatusOngoing
Mandated?Voluntary: Firm initiated
Recall NumberD-0182-2025
Event ID96014
BrandCIPROFLOXACIN
Generic NameCIPROFLOXACIN
ManufacturerCIPROFLOXACIN
Original Package?1
Active SubstanceCIPROFLOXACIN HYDROCHLORIDE
Drug RouteOPHTHALMIC
DistributionNationwide
Quantity136,181 bottles
Recall ReasonDefective 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
Drug ClassificationClass II
Drug Code Info20250115
Product NDC69315-308
Drug UPC0369315308028 0369315308059
Recall Initiation Date20241216
Report Date20250115
Classification Date20250103
AddressB-8 MIDC Industrial AreaWaluj District
Aurangabad, Maharashtra State,  N/A
India
Recalling FirmFDC Limited
Initial Notification Letter
Unique Ingredient Identifier4BA73M5E37
Drug Application NumberANDA077568
Structured Product Labeling (SPL ID)8217ec14-6498-4c35-a5a9-511b451b9459
Structured Product Labeling (SPL Set ID)545527e7-05c7-4dbf-ab32-b3fa463d55b0
Similar To

© 2022 Recall.Report / Contact / Privacy Policy

This site's data is aggregated programmatically and provided "as is" without any representations or warranties, express or implied.
Recall.report is not affiliated with the Consumer Product Safety Commision, FDA, or US government in any way.