Fresh Recalls

FDAClass II · Drug · Recall D-0566-2026 · Recalled June 10, 2026

CAREone recall — Guardian Drug Co. Inc.

Agency report date: June 10, 2026.

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
CAREone
Company / brand
Guardian Drug Co
Lot / serial / date codes
Lot #: 1716259, Exp 3/31/2029.
Distribution
U.S.A. Nationwide
Agency product description and boundaries

CAREone, ULTRA STRENGTH CALCIUM ANTACID, Calcium Carbonate 1000 mg, 72 chewable Tablets, Distributed by: FOODHOLD U.S.A, LLC, LANDOVER, MD 20785, NDC 72476-178-23.

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.

2. Agency hazard and consumer action

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

No consumer remedy instructions are supplied in this record. Check the official notice and listed company contact for the agency’s current instructions.

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

Affected product: CAREone

3. Open the official notice or contact

Official recall ID
D-0566-2026
Brand
Guardian Drug Co
Classification
Class II
Recall status
Ongoing
Initiated
Voluntary: Firm initiated

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 #: 1716259, Exp 3/31/2029.
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
Verify with the official sources:

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Source: U.S. Food & Drug Administration. Agency excerpts come from the public data feed and may omit tables or later changes; the linked government source is authoritative. Source last checked September 7, 2026 at 6:00 AM UTC. Record retrieved September 7, 2026 at 6:00 AM UTC.

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