Warning
Guardian Drug Co. Inc. Recalls GOODSENSE Ultra Strength
This is a Class II recall. This product may cause temporary health problems or pose a slight threat of a serious nature.
Source: FDA
WarningRecall #D-0575-2026Drug / Pharmaceutical
Guardian Drug Co. Inc. Recalls GOODSENSE Ultra Strength
Guardian Drug Co. Inc. · Class II — Moderate Risk
Product Description
GOODSENSE Ultra Strength, Antacid TABLETS, Calcium Carbonate 1000 mg, 72 Chewable Tablets, Distributed by: Geiss, Destin & Dunn, inc., Peachtree City, GA, NDC 50804-171-68.
Reason for Recall
Presence of foreign substance: small metallic particles in chewable tablets.
FDA Classification
Class II — Moderate Risk
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.
Distribution
U.S.A. Nationwide
Remedy
Consumers should stop using this product. Contact the recalling firm for further instructions regarding this product.
411 Press Analysis
A Class II FDA recall has been issued for a pharmaceutical product from Guardian Drug Co. Inc., initiated on May 28, 2026. Presence of foreign substance: small metallic particles in chewable tablets. The product was distributed in U.S.A. Nationwide. While not the highest severity, consumers should exercise caution and stop using the product until the recall is resolved.
Sources: FDA openFDA Enforcement Database
This recall appears in: Drug & Medical Product Contamination and Guardian Drug recalls.