GlaxoSmithKline recalls TUMS Antacid 160-count bottles due to glass mineral wool contamination. Consumers should stop using affected products immediately to avoid potential injury.
Presence of Foreign Substance: The foreign material is primarily comprised of glass mineral wool.
GlaxoSmithKline is recalling TUMS Antacid chewable tablets in 160-count bottles because they contain glass mineral wool. This foreign substance could cause injury if swallowed or inhaled.
The foreign material in these TUMS tablets is primarily glass mineral wool, which can be harmful if ingested or inhaled. This poses a risk of injury, especially if the tablets are chewed and swallowed.
Owners of TUMS Antacid 160-count bottles with the specific NDC code 0135-0118-14 and lot number HV6B are affected. Children and individuals with swallowing difficulties are at higher risk.
Check for TUMS Antacid chewable tablets in 160-count bottles with NDC code 0135-0118-14 and lot number HV6B. The product was distributed by GlaxoSmithKline Consumer Healthcare Holdings LLC in Warren, NJ.
Immediately stop using and discard any affected TUMS Antacid tablets to avoid potential injury from glass mineral wool.
TUMS Antacid, Calcium Carbonate USP 1000 mg, Assorted Fruit flavor, Chewable Tablets, 160-count bottles with NDC 0135-0118-14 and lot number HV6B.
Check for the NDC code 0135-0118-14 and lot number HV6B on the product label. The product was distributed by GlaxoSmithKline Consumer Healthcare Holdings LLC in Warren, NJ.
The recall record does not mention any replacement or refund options.
We’ve drafted a message you can send GlaxoSmithKline to request your refund or repair — edit it as you like.
Subject: Recall D-0075-2024 — GlaxoSmithKline GlaxoSmithKline Hello, I own a GlaxoSmithKline that is covered by recall D-0075-2024 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.
