Gaviscon (Alumina & Magnesium Trisilicate) Regular Strength Original Flavor Chewable Tablets, 80 mg & 14.2 mg, 100-count bottles, Distributed by: GlaxoSmithKline Consumer Healthcare, L.P., Moon Twp, PA 15108, UPC 3 0088-1175-47 8.
Reported: July 5, 2017 Initiated: June 12, 2017 #D-0926-2017
Product Description
Gaviscon (Alumina & Magnesium Trisilicate) Regular Strength Original Flavor Chewable Tablets, 80 mg & 14.2 mg, 100-count bottles, Distributed by: GlaxoSmithKline Consumer Healthcare, L.P., Moon Twp, PA 15108, UPC 3 0088-1175-47 8.
Reason for Recall
Superpotent Drug: high out-of-specification result for magnesium.
Details
- Recalling Firm
- Sanofi-Aventis U.S. LLC
- Units Affected
- 2980 bottles
- Distribution
- Nationwide in the USA, Puerto Rico, and the United Kingdom.
- Location
- Bridgewater, NJ
Frequently Asked Questions
What product was recalled? ▼
Gaviscon (Alumina & Magnesium Trisilicate) Regular Strength Original Flavor Chewable Tablets, 80 mg & 14.2 mg, 100-count bottles, Distributed by: GlaxoSmithKline Consumer Healthcare, L.P., Moon Twp, PA 15108, UPC 3 0088-1175-47 8.. Recalled by Sanofi-Aventis U.S. LLC. Units affected: 2980 bottles.
Why was this product recalled? ▼
Superpotent Drug: high out-of-specification result for magnesium.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on July 5, 2017. Severity: Low. Recall number: D-0926-2017.
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