7-Eleven antacid chewable tablets contain small metallic particles
24/7 life by 7-Eleven Extra Strength Antacid Tablets, calcium carbonate 750 mg, are being recalled because of the presence of small metallic particles in the chewable tablets.
The agency’s classification
FDA (Drugs): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 3/5 (High).
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
24/7 life BY 7-ELEVEN Extra Strength Antacid Tablets, calcium carbonate 750 mg, 96 chewable tablets, distributed by 7-Eleven of Irving, Texas, UPC 0 5254863573 2, are 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.
The affected lot is 1276119, expiring 1/31/2029. Distribution was USA nationwide.
Consumers who have the 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
- 24/7 life BY 7-ELEVEN, Extra strength Antacid Tablets, Calcium Carbonate 750 mg, 96 chewable tablets, DISTRIBUTED BY 7-ELEVEN, IRVING, TX 75063, UPC 0 5254863573 2.
- Manufacturer
- Guardian Drug Co. Inc.
- Category
- Drug — Antacid tablet
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 (2)
- Lot #: 1276119
- Exp 1/31/2029.
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 23 recalled by Guardian Drug Co. Inc. under a single FDA (Drugs) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
See all 23 products in this recall →Related recalls
Same manufacturer · Guardian Drug Co. Inc.
See all →- HighCareOne extra strength calcium antacid tablets contain metallic particles
FDA (Drugs) · 2026-06-10
- HighGoodSense ultra strength antacid tablets contain small metallic particles
FDA (Drugs) · 2026-06-10
- HighCareOne ultra strength antacid tablets contain small metallic particles
FDA (Drugs) · 2026-06-10
- HighEqualine extra strength antacid tablets contain small metallic particles
FDA (Drugs) · 2026-06-10
- HighGoodSense antacid chewable tablets contain small metallic particles
FDA (Drugs) · 2026-06-10
Same hazard · foreign object
See all →- ModerateGearharts Fine Chocolates Recalled Due to Broken Glass Foreign Object
FDA (Food) · 2026-10-28
- SeverePar Health Recalls Argatroban Injection Vials Due to Particulate Matter
FDA (Drugs) · 2026-10-28
- ModerateMetoclopramide Tablets Recalled Due to Presence of Foreign Tablets or Capsules
FDA (Drugs) · 2026-10-21
- ModerateTeva Recalls Metoclopramide Tablets Due to Foreign Object Presence
FDA (Drugs) · 2026-10-21
- ModerateStewart's Shops Vanilla Heavenly Medley Recalled for Metal Pieces
FDA (Food) · 2026-10-21
Similar recalls
- HighL. Perrigo Recalls Calcium Carbonate Antacid Tablets Due to Metal Particles
FDA (Drugs) · 2018-11-28
- ModerateCalcium Antacid (Calcium Carbonate) Recall Due to Blister Packaging Separation
FDA (Drugs) · 2024-11-27
- LowNovartis Recalls Maalox Extra Strength Antacid Tablets Due to Illegible Labeling
FDA (Drugs) · 2013-08-28
- ModerateDr. Reddy's Recalls Atorvastatin Calcium Tablets Due to Foreign Object
FDA (Drugs) · 2018-06-27
- LowNovartis Recalls Maalox Antacid Tablets Due to Illegible Packaging Labels
FDA (Drugs) · 2013-08-28
- LowNovartis Recalls Maalox Antacid Tablets Due to Illegible Labeling
FDA (Drugs) · 2013-08-28