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Home › Prescription medicine › Bausch Health Companies, Inc. — Omeprazole and…
The notice says to stop using the affected product — check the details below.
Subpotent Drug: Out of specification for assay
The Recall Registry rates this serious — FDA Class II: temporary or medically reversible health harm.
The recall notice tells people to stop using the affected product. Check the lot numbers below, and speak to your pharmacist or doctor about what to take instead — especially if this is something you take every day.
Who to contact: Recalling firm: Bausch Health Companies, Inc.
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.
Nationwide
This recall was issued by the U.S. Food and Drug Administration. The Recall Registry summarises it — always confirm the details at the source.
Their exact wording: “Bausch Health Companies, Inc. — 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 contai”
Worried about the other things in your house? You can write down what you have and be told if one is recalled — or, if you sell second-hand, check your whole stock at once.
Filed under: Prescription medicine