FreshRecalls

⚠ Data freshness notice: the most recent refresh of NHTSA was incomplete, so a very recent recall may be missing. Everything shown is accurate as of the last checked time on this page — for anything time-critical, confirm with the official sources linked below.

FDAClass II · Drug · Recalled June 10, 2026

GOODSENSE Ultra Strength 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-0575-2026
Brand
Guardian Drug Co
Classification
Class II
Recall status
Ongoing
Initiated
Voluntary: Firm initiated

Description

GOODSENSE Ultra Strength, Antacid TABLETS, Calcium Carbonate 1000 mg, 72 Chewable Tablets, Distributed by: Geiss, Destin & Dunn, inc., Peachtree City, GA, NDC 50804-171-68.

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 #: 1716089, expires: JAN- 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 23, 2026 at 11:04 PM UTC.

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