Startseite/Alle Rückrufe/FDA-D-0574-2026
FDA DrugsClass II

GOODSENSE Extra Strength, Antacid TABLETS, Calcium Carbonate 750 mg, 96 Chewable Tablets, Distributed by: Geiss, Destin & Dunn, inc., Peachtree City, GA, NDC 50804-129-22.

Veröffentlicht: 10. Juni 2026Rückruf-ID: D-0574-2026Kategorie: Arzneimittel & MedikamenteLand: Vereinigte Staaten
US
PharmaceuticalFDA DrugsUSUS

GOODSENSE Extra Strength, Antacid TABLETS, Calcium Carbonate 750 mg, 96 Chewable Tablets, Distributed by: Geiss, Destin & Dunn, inc., Peachtree City, GA, NDC 50804-129-22.

Recalling Firm: Guardian Drug Co. Inc.

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Mitteilung übersetzenTranslate notice text, hazard warnings, and descriptions into any supported language.

Grund für den Rückruf / Gefahr

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

Produktbeschreibung & Identifikation

GOODSENSE Extra Strength, Antacid TABLETS, Calcium Carbonate 750 mg, 96 Chewable Tablets, Distributed by: Geiss, Destin & Dunn, inc., Peachtree City, GA, NDC 50804-129-22.

Additional Source Details

FieldValue
CityDayton
StateNJ
Openfda › UniiH0G9379FGK
Openfda › RouteORAL
Openfda › Rxcui308915
Openfda › Spl id5ba7313a-c112-4187-9c25-cc91ba317547
Openfda › Brand nameGOODSENSE EXTRA STRENGTH ANTACID
Openfda › Spl set id2fcdeb06-17de-49d8-97bb-8d31e1c0c61f
Openfda › Package ndc50804-129-22
Openfda › Product ndc50804-129
Openfda › Generic nameCALCIUM CARBONATE
Openfda › Product typeHUMAN OTC DRUG
Openfda › Substance nameCALCIUM CARBONATE
Openfda › Manufacturer nameGoodSense
Openfda › Application numberM001
Openfda › Is original packagertrue
Event id99098
Address 12 Charles Ct
Code infoLot #: 1276118, expires: JAN- 2029.
Postal code08810-1508
Report date20260610
Product typeDrugs
Reason for recallPresence of foreign substance: small metallic particles in chewable tablets.
Voluntary mandatedVoluntary: Firm initiated
Recall initiation date20260528
Initial firm notificationLetter
Center classification date20260603

Consumer Action Protocol: What You Should Do Immediately

Safety Steps
1Verify Product Identifiers

Inspect the NDC code, batch number, or control number on your medicine bottle or blister packaging to confirm whether your unit is included.

2Isolate & Discontinue Use

Do not abruptly stop critical prescribed medication without physician advice. Contact your dispensing pharmacist immediately for a safe alternative.

3Claim Free Statutory Remedy

Under statutory consumer protection rules, consumers are entitled to a full refund, certified replacement, or free repair kit without needing the original sales receipt.

4Report Adverse Incidents

If you suffered an injury, illness, or property damage from this product, file an official incident report with regulatory authorities (FDA Drugs).

Your Legal Rights as a Consumer

Recalls are legally binding corrective safety actions overseen by statutory government bodies. Recalling entities are legally prohibited from charging consumers for official safety remedies. If a retailer or dealership refuses your recall remedy, notify the issuing regulatory agency immediately.

Frequently Asked Questions About This Recall

FAQ Guide

Q1:What should I do immediately if I own or bought GOODSENSE Extra Strength, Antacid TABLETS, Calcium Carbonate 750 mg, 96 Chewable Tablets, Distributed by: Geiss, Dest...?

Check the lot number and NDC on your prescription label. For essential medications, consult your doctor or dispensing pharmacist immediately before abruptly stopping your dose.

Q2:Can I get a full refund or free repair for this recall?

Yes. Recalling manufacturers and retail merchants are required under consumer protection regulations to offer a statutory remedy—typically a full refund, certified repair kit, or replacement unit.

Q3:Do I need my original sales receipt to claim a remedy or refund?

In most recall cases, no receipt is required. Because safety recalls are matters of public health and statutory compliance, retailers and manufacturers routinely issue refunds, store credit, or replacement kits upon presentation of the affected product or lot code.

Q4:Where can I verify official information for this safety alert?

This safety alert is aggregated directly from official regulatory agency records (FDA Drugs). You can click the 'Official Agency Alert' link on this page to view the primary government notice and contact the manufacturer directly.

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Übersicht

  • Rückrufendes UnternehmenGuardian Drug Co. Inc.
  • StatusOngoing
  • RisikostufeClass II
  • DistributionU.S.A. Nationwide
Recall Hazard Severity
High Alert (Class I)
Offizielle Behördenwarnung

📢 Warnung teilen

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🚨 SAFETY ALERT: Guardian Drug Co. Inc. - GOODSENSE Extra Strength, Antacid TABLETS, Calcium Carbonate 750 mg, 96 Chewable Tablets, Distributed by: Geiss, Destin & Dunn, inc., Peachtree City, GA, NDC 50804-129-22.

Check if your household is affected:
https://therecallfile.com/de/recalls/goodsense-extra-strength-antacid-tablets-calcium-carbonate-750-mg-96-c/FDA-D-0574-2026
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