Class II ยท Moderate risk
KIRKLAND Signature
Presence of foreign substance: small metallic particles in chewable tablets.
National Drug Code
Is NDC 63981-0171-80 recalled?
Kirkland Ultra Stregth Antacid 171AB · 265 TABLET in 1 BOTTLE (63981-171-80)
Yes — this exact package was recalled
1 FDA recall names the code 63981-0171-80 directly. A recall still applies to particular lot numbers — compare the lot on your package with the FDA notice below, and talk to your pharmacist before stopping a prescribed medication.
1 of these recalls is still ongoing.
- Active ingredient
- Calcium carbonate
- Strength
- CALCIUM CARBONATE 1000 mg/1
- Form
- Tablet · Oral
- Labeler
- Costco Wholesale Company
- Type
- Human OTC Drug
- Product code
- 63981-0171
Recalls naming this package
Where to find this code. The NDC is printed on the pharmacy label and on the manufacturer's carton, usually as three groups of digits after “NDC”. The last group is the package size — two bottles of the same medicine can differ only in that group, and a recall may cover one but not the other.
Other recalled products from this labeler
- 63981-0571 See recall 1
- 63981-0724 KIRKLAND SIGNATURE ALLERCLEAR D 24 HR Extended Release 1
- 63981-0795 Severe Cold and Flu Plus Congestion 1
- 63981-0847 kirkland signature aller fex 1
- 63981-0852 See recall 1
Free recall alerts
Know the day your medication is recalled
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