RecallRadar

FDA Drug recall D-850-2013

TUMS, Antacid/Calcium Supplement, ULTRA Strength 1000, Assorted Berries, 72 Chewable Tablets, GlaxoSmithKline, Moon Twp, PA 15108, NDC 0135…

On 2013-08-14 the FDA classified a Class III recall of TUMS, Antacid/Calcium Supplement, ULTRA Strength 1000, Assorted Berries, 72 Chewable Tablets, GlaxoSmithKline, Moon Twp, PA 15108, NDC 0135… by Glaxosmithkline, citing presence of Foreign Tablets/Capsules: Product labeled TUMS Ultra Assorted Berries 1000mg Chewable tables, may contain EX TUMS Assorted Berries 750mg tablets.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-850-2013
ClassificationClass III
Statusterminated
Initiated2013-07-18
Published2013-08-14
Last updated2026-09-13 11:51 UTC
CompanyGlaxosmithkline
DistributionUS

Product

TUMS, Antacid/Calcium Supplement, ULTRA Strength 1000, Assorted Berries, 72 Chewable Tablets, GlaxoSmithKline, Moon Twp, PA 15108, NDC 0135-0181-02

Reason

Presence of Foreign Tablets/Capsules: Product labeled TUMS Ultra Assorted Berries 1000mg Chewable tables, may contain EX TUMS Assorted Berries 750mg tablets

Identifiers

ndc0135-0118-01
ndc0135-0118-04
ndc0135-0118-14
ndc0135-0118-83
ndc0135-0180-01
ndc0135-0180-02
ndc0135-0180-14
ndc0135-0181-01
ndc0135-0181-02
ndc0135-0181-03
ndc0135-0181-05
ndc0135-0181-06
ndc0135-0181-07
ndc0135-0181-14
ndc0135-0228-01
ndc0135-0228-04
ndc0135-0228-05
ndc0135-0228-06
ndc0135-0228-07
ndc0135-0540-01
code_infoLot 3C11 and 3C11A

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-850-2013%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.