GlaxoSmithKline recalls TUMS Antacid tablets with glass mineral wool contamination. Consumers should stop using affected bottles to avoid potential injury from glass fragments.
Presence of Foreign Substance: The foreign material is primarily comprised of glass mineral wool.
GlaxoSmithKline is recalling TUMS Antacid tablets that contain glass mineral wool. This foreign substance could cause injury if swallowed or ingested.
The tablets contain glass mineral wool, a foreign substance that can break into sharp fragments. If swallowed, these fragments could cause cuts or lacerations in the mouth, throat, or digestive tract.
Owners of TUMS Antacid tablets in 72-count bottles with the specific NDC code 135-0181-02 are affected. Children and individuals with swallowing difficulties are at higher risk due to potential glass fragment injury.
Check for TUMS Antacid tablets in 72-count bottles with the NDC code 135-0181-02. The lot number HR5W and expiration date 09/30/2027 are also associated with this recall.
Immediately stop using the recalled TUMS Antacid tablets as they contain glass mineral wool that could cause injury if swallowed.
TUMS Antacid, Calcium Carbonate USP 1000 mg, Assorted Berries flavor, Chewable Tablets in 72-count bottles with NDC 135-0181-02.
Check for the NDC code 135-0181-02 on the bottle, which is associated with the recall. The lot number HR5W and expiration date 09/30/2027 are also part of the affected batch.
Immediately stop using the product and contact GlaxoSmithKline Consumer Healthcare Holdings LLC for further instructions.
We’ve drafted a message you can send GlaxoSmithKline to request your refund or repair — edit it as you like.
Subject: Recall D-0076-2024 — GlaxoSmithKline GlaxoSmithKline Hello, I own a GlaxoSmithKline that is covered by recall D-0076-2024 from GlaxoSmithKline. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
