Recall details are shown for all drugs with the same active ingredient as the chosen drug. Please read the Product Description carefully and consult the distribution map to determine if the recall effects you.
Product Description: Omeprazole and Sodium Bicarbonate For Oral Suspension 40mg/1,680mg, This packet contains 40mg of omeprazole and 1,680mg of sodium bicarbonate, Directions for Use: Empty packet contents into a small cup containing 1 to 2 tablespoons of WATER. DO NOT USE OTHER LIQUIDS OR FOODS. Stir well and drink immediately. Rx Only, Distributed by: Oceanside Pharmaceuticals, a division of Bausch Health US, LLC, Bridgewater, NJ 08807, NDC 68682-991-30.
Product Quantity: 3,600 cartons
Identifiers: Lot #0013R; Exp. 01/2026
Recall Reason: Subpotent Drug: Out of specification for assay
Initiation Date: 02/02/2024 • Recall Number: D-0355-2024
Report Date: 03/06/2024 • Reporting Firm: Bausch Health Companies, Inc.
Product Description: Omeprazole Delayed-Release Capsules, USP, 20 mg, Rx Only, 1000 Capsules per bottle, Distributed by: Kremers Urban Pharmaceuticals Inc. Princeton, NJ 08540, USA, NDC: 62175-118-43
Product Quantity: 3867 bottles
Identifiers: Lot Number 59627; Expiration Date 02/2014
Recall Reason: Failed Tablet/Capsule Specification: some capsules over time do not meet or are suspected to not meet the specification for acid resistance.
Initiation Date: 09/16/2013 • Recall Number: D-009-2014
Report Date: 11/27/2013 • Reporting Firm: Kremers Urban Pharmaceuticals, Inc.