Fresh Recalls

GOODSENSE Ultra Strength: recall status

Notice names this product. Guardian Drug Co’s GOODSENSE Ultra Strength is named in FDA Class II recall D-0575-2026. Your particular item is not yet verified. Compare the identifiers and exclusions in the notice before deciding whether it applies. Agency-reported hazard: Presence of foreign substance: small metallic particles in chewable tablets. Identifying details: Lot #: 1716089, expires: JAN- 2029.. Status: Ongoing.

1. Compare your item

This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.

Product named
GOODSENSE Ultra Strength
Company / brand
Guardian Drug Co
Lot / serial / date codes
Lot #: 1716089, expires: JAN- 2029.
Distribution
U.S.A. Nationwide
Agency product description and boundaries

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.

Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.

If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.

Brand
Guardian Drug Co

Recalls naming this model

FDA Class II · Drug · June 10, 2026

GOODSENSE Ultra Strength recall — Guardian Drug Co. Inc.

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

Company / brand: Guardian Drug Co

Affected product: GOODSENSE Ultra Strength

Official ID D-0575-2026 · Official record ↗

See all Guardian Drug Co recalls →

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Compiled from connected official public-domain government data. Sources last checked September 7, 2026 at 6:00 AM UTC.