CareOne extra strength calcium antacid tablets contain metallic particles
CareOne Extra Strength Calcium Antacid, calcium carbonate 750 mg, is being recalled because of the presence of small metallic particles in the chewable tablets.
What this means for you
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: Metallic particles in a chewable tablet are a physical hazard capable of causing injury, a risk of harm with no injuries reported in the source.
Plain-English summary
CAREone Extra Strength Calcium Antacid, calcium carbonate 750 mg, 96 chewable tablets, distributed by Foodhold U.S.A., LLC of Landover, Maryland, NDC 72476-127-80, is being recalled.
The stated reason is the presence of a foreign substance: small metallic particles in the chewable tablets. The FDA classified the action as Class II.
Affected lots are 1276118 and 1276119, expiring January 2029. Distribution was USA nationwide.
Consumers who have an affected lot should stop using it and return it to the place of purchase. Anyone injured after taking the tablets should seek medical advice.
The recalled product
- Product
- EXTRA STRENGTH ANTACID (CALCIUM CARBONATE)
- Brand
- EXTRA STRENGTH ANTACID
- Manufacturer
- Guardian Drug Co. Inc.
- Category
- Drug — Antacid tablet
- Hazard
- foreign-object
- metallic-particles
- physical-hazard
- class-ii
- otc-drug
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (3)
- Lot #: 1276118
- 1276119
- expires: JAN 2029.
UPCs (2)
- 0341520317309
- 0341520312120
Distribution
Distributed nationwide across the United States.
Related recalls
Same category
- ModerateQuality Choice Earwax Removal Kit Carbamide Peroxide Subpotent Drug Recall
FDA (Drugs) · 2026-07-22
- ModerateFamily Wellness Carbamide Peroxide Earwax Removal Kit Subpotent Drug
FDA (Drugs) · 2026-07-22
- SevereCleviprex Injectable Emulsion Recall Due to Sterility Assurance Concerns
FDA (Drugs) · 2026-07-22
- ModerateLeader Carbamide Peroxide Earwax Removal Kit Recalled for Subpotency
FDA (Drugs) · 2026-07-22
- ModerateNystatin Cream Recall Due to Low Potency Test Results
FDA (Drugs) · 2026-07-22