Reported Jul 18, 2012 · Terminated
Nexium (esomeprazole magnesium) Delayed-Release Capsules, 40 mg, 1000-count bottle, Rx only, Manufactured for:…
ASTRA ZENECA LP
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: ASTRA ZENECA Lp · 1800 CONCORD PIKE · WILMINGTON, DE · 19803-2902
Is this the product you have?
- Nexium (esomeprazole magnesium) Delayed-Release Capsules, 40 mg, 1000-count bottle, Rx only
- Manufactured forAstraZeneca LP, Wilmington, DE 19850
- By
AstraZeneca ABS-151 85 SodertaljeSwedenNDC 0186-5040-85UPC 3 0186-5040-85 0
- Lot codes and dates
Lot #: H008328Exp 11/14
- Amount recalled
- 2,556 bottles
Where it was sold
- Nationwide
Why it was recalled
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.
This product is unlikely to cause harm, but it breaks a safety or labelling rule.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
Free recall alerts
Get alerted about new ASTRA ZENECA LP recalls
One email when a matching recall is published. No account, no cost, unsubscribe in one click.
We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.