PlainRecalls
ModerateClass IICompleted

FDA Drug recall · Reported November 8, 2023

TUMS Antacid, Calcium Carbonate USP 1000 mg, Peppermint flavor, chewable tablets, 72-count bottle, Dist. by: GSK CH, Warren, NJ 07059. NDC: 0135-0228-06, UPC 3-0766-0745-85-3

Presence of Foreign Substance: The foreign material is primarily comprised of glass mineral wool.

Recall #
D-0073-2024
Affected scope
N/A
Initiated
December 2, 2022
Verify with FDA Drug →
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GlaxoSmithKline Consumer Healthcare Holdings LLC recalled TUMS Antacid, Calcium Carbonate USP 1000 mg, Peppermint flavor, chewable tablets, 72-coun… - a moderate-severity action.

TUMS Antacid, Calcium Carbonate USP 1000 mg, Peppermint flavor, chewable tablets, 72-coun… was recalled by GlaxoSmithKline Consumer Healthcare Holdings LLC in November 8, 2023. Reason: Presence of Foreign Substance: The foreign material is primarily comprised of glass mineral wool.. Check the official notice for the remedy. Verify recall #D-0073-2024 with the FDA Drug before acting.

The recall

GlaxoSmithKline Consumer Healthcare Holdings LLC issued this moderate-severity FDA Drug recall-Presence of Foreign Substance: The foreign material is primarily comprised of glass mineral wool..

Moderate
severity level
Class II
classification
November 8, 2023
reported

Sourced from official FDA Drug enforcement records. Verify recall #D-0073-2024 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.

Recall Insight

This recall's affected scope, documented in the Recall Profile below, stays within a single-region or limited-distribution footprint. Distribution scope (see Distribution below) directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.

Within the same product category the archive holds 6 closely related recalls, 1 from FDA Drug - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.

Children & Baby Products recalls over time

Where this recall sits in its category - 3,781 children & baby products recalls on record

0100200300400500600 20052008201120142017202020232026 196
Severity1906864652High severity (most serious)Moderate severityLow severity
Where this agency-classified recall sits among FDA Class I/II/III notices

Of 88,244 recalls with an agency hazard classification, 19,068 are high severity, 64,652 moderate, and 4,524 low. A further 16,179 CPSC/NHTSA recalls have no agency class and are excluded from this split. This recall is classified moderate severity.

Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.

Product description

TUMS Antacid, Calcium Carbonate USP 1000 mg, Peppermint flavor, chewable tablets, 72-count bottle, Dist. by: GSK CH, Warren, NJ 07059. NDC: 0135-0228-06, UPC 3-0766-0745-85-3

Reason for recall

Presence of Foreign Substance: The foreign material is primarily comprised of glass mineral wool.

Recall Profile

Structured summary of the FDA Drug recall record
Attribute Value
Agency U.S. Food and Drug Administration
Severity class Moderate (Class II)
Status Completed
Recall number D-0073-2024
Date reported November 8, 2023
Date initiated December 2, 2022
Recalling firm GlaxoSmithKline Consumer Healthcare Holdings LLC
Firm location Saint Louis, MO
Affected scope N/A
Distribution Nationwide within the United States

Profile values are sourced directly from the official FDA Drug enforcement record. Source: U.S. Food and Drug Administration.

What to do with this recall

Match your product against the recall record, then act on the agency remedy.

  • Check the recall number (D-0073-2024) and product description against the item you own. Search the archive
  • Confirm the current status with FDA Drug before acting, recall details can be updated.
  • Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next

This page summarizes the official FDA Drug record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.

Frequently Asked Questions

What product was recalled?
TUMS Antacid, Calcium Carbonate USP 1000 mg, Peppermint flavor, chewable tablets, 72-count bottle, Dist. by: GSK CH, Warren, NJ 07059. NDC: 0135-0228-06, UPC 3-0766-0745-85-3. Recalled by GlaxoSmithKline Consumer Healthcare Holdings LLC. Units affected: N/A.
Why was this product recalled?
Presence of Foreign Substance: The foreign material is primarily comprised of glass mineral wool.
Which agency issued this recall?
This recall was issued by the FDA Drug on November 8, 2023. Severity: Moderate. Recall number: D-0073-2024.
Where was the recalled product distributed?
Distribution: Nationwide within the United States.
Should I stop using a recalled medication or medical device?
Do not stop using a recalled medication or device without consulting your healthcare provider first, as abruptly discontinuing treatment could pose its own health risks. Your doctor can advise on alternatives or whether the recall applies to your specific product lot. Check the recall number and lot information against your product packaging.

Nationwide recalls with similar severity or category timing

Drug and device notices outside this firm and state, matched by severity timing and product category.

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This recall: FDA Drug, reported November 8, 2023. Severity classes follow each agency's own taxonomy; related-recall context is computed across the full archive.

Methodology · Corrections · Archive as of August 2026