December 2023 FDA Recall Bupropion Hydrochloride by Rising Pharma Holding, Inc.
D-0222-2024 - Presence of Foreign Tablets/Capsules

This Class II drug recall was voluntarily initiated by Rising Pharma Holding, Inc. on December 29, 2023 for the product Bupropion Hydrochloride. The FDA reported the reason for recall as presence of foreign tablets/capsules. The product was distributed Nationwide and the recall is currently ongoing.

Recall Number: D-0222-2024

Reason for Recall
Presence of Foreign Tablets/Capsules
Initiated
12-29-2023
Reported
01-17-2024
Quantity
47,976 bottles

Recall Profile & Regulatory Data

Class II - is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Rising Pharma Holding, Inc.
Nationwide within the United States
buPROPion Hydrochloride Extended-Release Tablets, USP (XL) 150mg, 30-count bottles, Rx Only, Manufactured for: Rising Pharma Holdings, Inc. East Brunswick, NJ 08816 Manufactured by: Graviti Pharmaceuticals Pvt. Ltd. Telangana - 502307, INDIA, NDC 16571-862-03

Batch or Lot Expiration Information

Lot# : BPA123098A, Exp. Date 06/2025