FDA recall, , Moderate risk
Guardian Drug Antacid Tablets
Antacid tablets contain small metallic particles.
Summary by Recall Canary from the FDA notice
What happened
Guardian Drug Co. Inc. of Dayton, New Jersey, recalled multiple brands of chewable antacid tablets because they may contain small metallic particles. The recall began May 28, 2026, and was added to the FDA's Enforcement Report on June 3, 2026. Products include HyVee Ultra Strength Antacid, Haleon Calcium Carbonate Tums Antacid, Careone Extra Strength Calcium Antacid, TopCare health, Goodsense, Discount drug mart, and other products distributed nationwide.
What to do
We don't have product-specific instructions for this recall. FDA's general advice for medicine recalls:
- Check the FDA or company notice for instructions specific to this product.
- Ask your pharmacist or doctor whether your lot is affected and what to do.
Is yours affected?
Match your product and all the details in one listed combination.
A UPC is the number printed under a barcode. An NDC (National Drug Code) is usually printed on the drug's label.
Discount drug mart, Extra Strength, Antacid Tablets, Calcium Carbonate
- Strength
- 750 mg
- UPC
- 0 93351 03992 8
- Lot code
- 1276118
HyVee, Ultra Strength Antacid, Calcium Carbonate
- Strength
- 1000 mg
- UPC
- 0 75450 82514 5
- Lot code
- 1716089
Haleon Calcium Carbonate Tums Antacid, Assorted Fruit Tablets
- Strength
- 1000 mg
- UPC
- 3 07660 74610 2
- Lot code
- 1096075
- 1096076
- 1096077
- 1096078
- Strength
- 750 mg
- UPC
- 3 0766 3072 10 9
- Lot code
- 1076169
CAREone, Extra Strength Calcium Antacid, Calcium Carbonate
- Strength
- 750 mg
- NDC
- 72476-127-80
- Lot code
- 1276118
- 1276119
HyVee, Extra Strength Antacid, Calcium Carbonate
- Strength
- 750 mg
- UPC
- 0 75450 82497 1
- Lot code
- 1276119
TopCare health, Ultra Strength, Antacid Tablets, Calcium Carbonate
- Strength
- 1000 mg
- NDC
- 76162-129-68
- Lot code
- 1716089
Goodsense Ultra Strength, Antacid Tablets, Calcium Carbonate
- Strength
- 1000 mg
- NDC
- 50804-171-68
- Lot code
- 1716089
Extra strength Antacid Calcium Carbonate
- Strength
- 750 mg
- UPC
- 0 98437 24361 9
- Lot code
- 1276118
Equaline extra strength, antacid tablets, calcium carbonate
- Strength
- 750 mg
- NDC
- 41163-129-22
- Lot code
- 1276118
CAREone, Ultra Strength Calcium Antacid, Calcium Carbonate
- Strength
- 1000 mg
- NDC
- 72476-178-23
- Lot code
- 1716259
Equaline ultra strength, antacid tablets, calcium carbonate
- Strength
- 1000 mg
- NDC
- 41163-171-68
- Lot code
- 1716089
Goodsense Extra Strength, Antacid Tablets, Calcium Carbonate
- Strength
- 750 mg
- NDC
- 50804-129-22
- Lot code
- 1276118
Good Neighbor Pharmacy, extra strength Antacid Calcium Carbonate
- Strength
- 1000 mg
- NDC
- 24385-595-23
- Lot code
- 1716089
- Strength
- 750 mg
- NDC
- 24385-106-80
- Lot code
- 1276118
Market Basket Antacid Calcium Carbonate
- Strength
- 1000 mg
- UPC
- 0 49705 83149 6
- Lot code
- 1716089
Family Wellness, Ultra Strengt, Antacid Tablets, Calcium Carbonate
- Strength
- 1000 mg
- NDC
- 55319-171-68
- Lot code
- 1716089
- UPC
- 0 32251-92282-4
- Lot code
- 1716259
H.E.B Extra Strength Calcium Carbonate Antacid Tablets, Calcium Carbonate
- Strength
- 750 mg
- NDC
- 37808-136-22
- Lot code
- 1276118
TopCare health, Extra Strength, Antacid Tablets, Calcium Carbonate
- Strength
- 750 mg
- NDC
- 76162-128-22
- Lot code
- 1276119
24/7 life By 7-Eleven, Extra strength Antacid Tablets, Calcium Carbonate
- Strength
- 750 mg
- UPC
- 0 5254863573 2
- Lot code
- 1276119
Harris Teeter, Ultra Strength Antacid, Calcium Carbonate
- Strength
- 1000 mg
- UPC
- 0 72036-73108-1
- Lot code
- 1716089
KIRKLAND Signature, Ultra Strength Antacid, Calcium Carbonate
- Strength
- 1000 mg
- NDC
- 63981-171-80
- Lot code
- 1716059
- 1716060
- 1716061
- 1716062
- 1716063
- 1716218
- 1716219
- 1716228
- 1716229
- 1716238
- 1716258
Recall details
- Company began the recall
- Sold in
U.S.A. Nationwide
- Company
- Guardian Drug Co. Inc.Dayton, New Jersey
- Hazard
- Foreign object
- Risk
Moderate risk
Taking it may cause short-term health problems, or ones that treatment can reverse. Serious harm is unlikely.
FDA Class II recall · How risk is rated
- Event ID
- 99098
- Recall numbers
- D-0557-2026 to D-0579-2026
Timeline
FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.
Company began the recall
Added to FDA's Enforcement Report · Classified by FDA
Listed on Recall Canary
In FDA's weekly enforcement report
Summary updated
