RecallDepth
Class III Ongoing

Pregabalin Capsules 50mg, 1000-count bottle, Rx Only, Manufactured for: Rising Pharma Holdings, Inc., East Brunswick, NJ 08816, Manufactured by: Laurus Labs Limited, Anakapalli-531011, India, NDC 64980-411-10

This recall is currently active, issued June 12, 2024. It was issued by Rising Pharma Holding, Inc..

Company
Rising Pharma Holding, Inc.
Recall Initiated
May 16, 2024
Posted
June 12, 2024
Recall Number
D-0541-2024
Voluntary / Mandated
Voluntary: Firm initiated
Firm Location
East Brunswick, NJ, United States
Official Source
View on FDA website ↗

Reason for Recall

Presence of Foreign Tablets/Capsules: Complaint received from a re-packager, American Health Packaging (AHP), where a foreign tablet was discovered in one of the bottles during packaging set up. Tablet identified as pantoprazole tablet 20mg.

Distribution

Nationwide in the USA

Lot / Code Info

Lot: 23132611, Exp 07/31/2026

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