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.
Reported: June 24, 2015 Initiated: June 10, 2015 #D-1141-2015
Product Description
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.
Reason for Recall
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.
Details
- Recalling Firm
- AstraZeneca Pharmaceuticals LP
- Units Affected
- 34,524 bottles
- Distribution
- Nationwide to wholesalers for further distribution at the retail level.
- Location
- Wilmington, DE
Frequently Asked Questions
What product was recalled? ▼
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.. Recalled by AstraZeneca Pharmaceuticals LP. Units affected: 34,524 bottles.
Why was this product recalled? ▼
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.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on June 24, 2015. Severity: Moderate. Recall number: D-1141-2015.
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