Guardian Drug Co. Inc. recalls GOODSENSE Ultra Strength
- Recalling company
- Guardian Drug Co. Inc.
- Product
- 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
- Presence of foreign substance: small metallic particles in chewable tablets.
- Classification
- Class II – may cause temporary or medically reversible health consequences
- Recall date
- May 28, 2026
- Reported
- Jun 10, 2026
- Distribution
- U.S.A. Nationwide
- Status
- Ongoing
- Lot / codes
- Lot #: 1716089, expires: JAN- 2029.
- Company location
- Dayton, NJ
- Recall type
- Voluntary: Firm initiated
- Recall number
- D-0575-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number D-0575-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.