RecallRadar

FDA Drug recall D-1410-2012

Nexium (esomeprazole magnesium) Delayed-Release Capsules, 40 mg, 1000-count bottle, Rx only, Manufactured for: AstraZeneca LP, Wilmington,…

On 2012-07-18 the FDA classified a Class III recall of Nexium (esomeprazole magnesium) Delayed-Release Capsules, 40 mg, 1000-count bottle, Rx only, Manufactured for: AstraZeneca LP, Wilmington,… by Astra Zeneca, citing adulterated Presence of Foreign Tablets/Capsules: Some bottles may contain a small number of Nexium 20 mg capsules intended for the Japanese market in addtion to Nexium 40 mg caps….

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-1410-2012
ClassificationClass III
Statusterminated
Initiated2012-07-02
Published2012-07-18
Last updated2026-09-13 11:51 UTC
CompanyAstra Zeneca
DistributionUS

Product

Nexium (esomeprazole magnesium) Delayed-Release Capsules, 40 mg, 1000-count bottle, Rx only, Manufactured for: AstraZeneca LP, Wilmington, DE 19850; By: AstraZeneca AB, S-151 85 Sodertalje, Sweden, NDC 0186-5040-85, UPC 3 0186-5040-85 0.

Reason

Adulterated Presence of Foreign Tablets/Capsules: Some bottles may contain a small number of Nexium 20 mg capsules intended for the Japanese market in addtion to Nexium 40 mg capsules.

Identifiers

upc301865040850
ndc0186-5020-31
ndc0186-5020-54
ndc0186-5020-82
ndc0186-4010-01
ndc0186-4010-02
ndc0186-4020-01
ndc0186-4040-01
ndc0186-4040-02
ndc0186-5040-31
ndc0186-5040-35
ndc0186-5040-55
ndc0186-5040-85
ndc0186-5040-54
ndc0186-5040-82
ndc0186-5040-05
ndc0186-4025-01
ndc0186-4025-02
ndc0186-4050-01
code_infoLot #: H008328, Exp 11/14

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-1410-2012%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.