24/7 life BY 7-ELEVEN Antacid Tablets Recall
Areazine synthesizes this FDA recall directly from FDA's official public data feed. See our methodology for full source attribution and refresh cadence.
Guardian Drug Co. Inc. is recalling one lot of 24/7 life BY 7-ELEVEN Extra strength Antacid Tablets due to the presence of small metallic particles.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on July 9, 2026 and geographically references United States. Its severity classification of "medium" signals how the issuing agency weighs the risk of harm if no action is taken - "critical" and "high" tier alerts typically carry direct consumer actions, while "medium" and "low" tend toward informational guidance or monitoring advisories. The category it belongs to - FDA Recalls - determines the consumer-protection framework behind it, which shapes what remedies (refunds, replacements, repairs, or the recall itself) are available to affected consumers and which agency holds statutory responsibility for enforcement.
Most readers skim a notice like this, check whether they are personally affected, and move on. The more useful lens is to verify its scope, source, and timestamp, then compare related notices without assuming that one record proves a broader trend.
Areazine pairs this record with the original agency URL so you can check the primary source before acting. Its related labels are recall, product-safety, fda, Drugs.
What Happened
Guardian Drug Co. Inc. initiated a voluntary recall of certain antacid tablets after discovering the presence of foreign substance consisting of small metallic particles in chewable tablets.
Which Products Are Affected
The recall covers 24/7 life BY 7-ELEVEN, Extra strength Antacid Tablets, Calcium Carbonate 750 mg, 96 chewable tablets, distributed by 7-Eleven, Irving, TX 75063, with UPC 0 5254863573 2. Affected product is identified by Lot #: 1276119, Exp 1/31/2029. Distribution was nationwide in the U.S.A.
What You Should Do
Consumers possessing the recalled lot should not use the product.
Why This Matters
The Class II recall involves a drug product distributed nationwide that may contain metallic particles.
Source
FDA recall number D-0563-2026 (event ID 99098).
Original source: FDA Official Notice ↗
Related FDA Recalls
All FDA Recalls →Nationwide notices with similar length or severity timing 8
Two Areazine-derived peer sets for this FDA recall: nearest notices by body length and by same severity near the same agency date. Peers come from other categories so they are not the same-feed Related list above.
Similar body length
Nearest notices by article body length (807 characters here).
Similar severity timing
Same severity (medium) notices issued closest in time to July 9, 2026.
Frequently Asked Questions
Common questions about this FDA recall.