FDAFDA · Food and drugs·Recall number D-1141-2015
NEXIUM¿ (esomeprazole magnesium), Delayed-Release capsules, 20 mg, 30-count bottle, Rx only, Manufactured for AstraZeneca LLC, Wilmington, Distributed by AstraZeneca, AB, Sodertalje, Sweden. NDC 00186-5020-31.
Published June 24, 2015 · Recall initiated: June 10, 2015
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
Presence of Foreign Tablets/Capsules: Confimed customer compliant by a retail pharmacist that an unopened bottle labeled as NEXIUM¿ capsules contained 60 SEROQUEL¿ XR tablets.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- AstraZeneca Pharmaceuticals LP
- Distributor
- Nationwide to wholesalers for further distribution at the retail level.
- Lot
- Lot # FC0064; Exp. 05/17
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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