[pending] KIRKLAND ULTRA STREGTH ANTACID 171AB (CALCIUM CARBONATE)
Pending LLM rewrite. Source: FDA_DRUG D-0557-2026.
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: Pending LLM scoring against the rubric.
Plain-English summary
Presence of foreign substance: small metallic particles in chewable tablets.
The recalled product
- Product
- KIRKLAND ULTRA STREGTH ANTACID 171AB (CALCIUM CARBONATE)
- Brand
- KIRKLAND ULTRA STREGTH ANTACID 171AB
- Manufacturer
- Guardian Drug Co. Inc.
- Category
- Drug — Drugs
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 (13)
- Lot#: 1716059
- 1716060
- 1716061
- 1716062
- 1716063
- 1716218
- 1716219
- 1716228
- 1716229
- 1716238
- Exp 2/28/2029
- 1716258
- Exp 3/31/2029.
Distribution
Distributed nationwide across the United States.
Related recalls
Same category
- CriticalWarfarin Tablets Recalled After Mix-Up Between 2.5 mg and 5 mg Strengths
FDA (Drugs) · 2026-07-21
- ModerateFDA Recalls Pred Mild Ophthalmic Suspension Due to Failed Stability Specifications
FDA (Drugs) · 2026-06-03
- ModerateNicotine Transdermal System Patches Recalled for Oxidative Impurity Specification Failure
FDA (Drugs) · 2026-06-03
- ModerateGas-X Simethicone 125 mg softgels recall for incomplete labeling
FDA (Drugs) · 2026-05-27
- ModerateVitamin B-Complex, Vitamin C & Folic Acid Dietary Supplement Oral Liquid
FDA (Drugs) · 2026-05-27