Class III
Terminated
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.
This recall has been terminated (originally issued July 18, 2012).
- Company
- Astra Zeneca Lp
- Recall Initiated
- July 2, 2012
- Posted
- July 18, 2012
- Recall Number
- D-1410-2012
- Voluntary / Mandated
- Voluntary: Firm initiated
- Quantity
- 2,556 bottles
- Firm Location
- WILMINGTON, DE, United States
- Official Source
- View on FDA website ↗
Reason for Recall
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.
Distribution
Nationwide.
Lot / Code Info
Lot #: H008328, Exp 11/14
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