FDA Drug recall D-0074-2024
TUMS Antacid, Calcium Carbonate USP 1000 mg, Peppermint flavor, chewable tablets, packaged in 12-count roll, Dist. by: GSK CH, Warren, NJ 0…
- FDA Drug
- Class II
- completed
- Published 2023-11-08
On 2023-11-08 the FDA classified a Class II recall of TUMS Antacid, Calcium Carbonate USP 1000 mg, Peppermint flavor, chewable tablets, packaged in 12-count roll, Dist. by: GSK CH, Warren, NJ 0… by Glaxosmithkline Consumer Healthcare Holdings, citing presence of Foreign Substance: The foreign material is primarily comprised of glass mineral wool.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-0074-2024 |
| Classification | Class II |
| Status | completed |
| Initiated | 2022-12-02 |
| Published | 2023-11-08 |
| Last updated | 2026-09-13 11:52 UTC |
| Company | Glaxosmithkline Consumer Healthcare Holdings |
| Distribution | US |
Product
TUMS Antacid, Calcium Carbonate USP 1000 mg, Peppermint flavor, chewable tablets, packaged in 12-count roll, Dist. by: GSK CH, Warren, NJ 07059. NDC: 0135-0228-01, UPC 3-0766-0746-80-5
Reason
Presence of Foreign Substance: The foreign material is primarily comprised of glass mineral wool.
Identifiers
| upc | 307660746805 |
|---|---|
| ndc | 0135-0118-01 |
| ndc | 0135-0118-04 |
| ndc | 0135-0118-14 |
| ndc | 0135-0118-83 |
| ndc | 0135-0180-01 |
| ndc | 0135-0180-02 |
| ndc | 0135-0180-14 |
| ndc | 0135-0181-01 |
| ndc | 0135-0181-02 |
| ndc | 0135-0181-03 |
| ndc | 0135-0181-05 |
| ndc | 0135-0181-06 |
| ndc | 0135-0181-07 |
| ndc | 0135-0181-14 |
| ndc | 0135-0228-01 |
| ndc | 0135-0228-04 |
| ndc | 0135-0228-05 |
| ndc | 0135-0228-06 |
| ndc | 0135-0228-07 |
| ndc | 0135-0540-01 |
| ndc | 0766-0746-80 |
| code_info | Lot #: HA7G, Exp. Date 8/31/2027 |
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: completed.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0074-2024%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.