FDAFDA · Food and drugs·Recall number D-1410-2012
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.
Published July 18, 2012 · Recall initiated: July 2, 2012
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
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.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- NEXIUM
- Manufacturer
- ASTRA ZENECA Lp
- Distributor
- Nationwide.
- UPC
- 301865040850
- Lot
- Lot #: H008328, Exp 11/14
- Risk classification
- Class III
- Area (FDA)
- drug
- Country
- United States
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