TUMS — Class III drug recall D-850-2013
Terminated recall by GlaxoSmithKline, LLC., reported 2013-08-14, distributed nationwide. Presence of Foreign Tablets/Capsules: Product labeled TUMS Ultra Assorted Berries 1000mg Chewable tables, may
| Recall number | D-850-2013 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | GlaxoSmithKline, LLC., Zebulon, NC, United States |
| Recall initiated | 2013-07-18 |
| Classified | 2013-08-07 |
| Reported by FDA | 2013-08-14 |
| Terminated | 2016-05-18 |
| Distributed | Nationwide (US) |
| Quantity | 300,480 bottles |
| Reason classes | labeling |
| NDC | 00135-0118, 00135-0118-01, 00135-0118-04, 00135-0118-14, 00135-0118-83, 00135-0180, 00135-0180-01, 00135-0180-02, 00135-0180-14, 00135-0181, 00135-0181-01, 00135-0181-02, 00135-0181-03, 00135-0181-05, 00135-0181-06, 00135-0181-07, 00135-0181-14, 00135-0228, 00135-0228-01, 00135-0228-04, 00135-0228-05, 00135-0228-06, 00135-0228-07, 00135-0540, 00135-0540-01 |
| Lot numbers | 3C11, 3C11A |
Product
TUMS, Antacid/Calcium Supplement, ULTRA Strength 1000, Assorted Berries, 72 Chewable Tablets, GlaxoSmithKline, Moon Twp, PA 15108, NDC 0135-0181-02
Reason for recall
Presence of Foreign Tablets/Capsules: Product labeled TUMS Ultra Assorted Berries 1000mg Chewable tables, may contain EX TUMS Assorted Berries 750mg tablets
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-850-2013. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.