FreshRecalls

FDAClass II · Drug · Recalled June 10, 2026

HALEON CALCIUM CARBONATE TUMS ANTACID recall — Guardian Drug Co. Inc.

Hazard: Presence of foreign substance: small metallic particles in chewable tablets.

Class II: may cause temporary or medically reversible health consequences.

View the official FDA enforcement record (openFDA) ↗

Official recall ID
D-0558-2026
Brand
Guardian Drug Co
Classification
Class II
Recall status
Ongoing
Initiated
Voluntary: Firm initiated

Description

HALEON CALCIUM CARBONATE TUMS ANTACID, Assorted Fruit Tablets, 1000 mg, 160-count bottle, Haleon, Warren, NJ 07059, UPC 3 07660 74610 2.

Affected products

Companies & origin

Recalling firm location
Dayton, NJ, United States
Firm address
2 Charles Ct, 08810-1508

Identifying details (verbatim from the notice)

Product codes / lots
Lot #: 1096075, 1096076, 1096077, 1096078, Exp 1/31/2029.
Distribution
U.S.A. Nationwide
Firm notified the public via
Letter
FDA event ID
99098
Recall initiated
May 28, 2026
FDA classified
June 3, 2026
FDA report date
June 10, 2026

Source: U.S. Food & Drug Administration. This page mirrors the official public-domain record verbatim; the linked government source is authoritative. Source last checked July 24, 2026 at 12:00 AM UTC.

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