drugs Class II Updated 2014-09-03

Alkermes, Inc. recalls VIVITROL (naltrexone for extended-release injectable suspens

Recalled Product

VIVITROL (naltrexone for extended-release injectable suspension); 380 mg vial NDC 65757-300-01; RX Only Manufactured and marketed by Alkermes, Inc., Waltham, MA 02451.

Hazard / Issue

Customer complaints for failure to deliver the dose.

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: Batch Number: 412-3732AA; expiration date 07/2016 (NDC# 65757-302-02; Kit Pacaging Lot Number: 2013-021; expiration date 07/2016 (NDC# 65757-300-01.
View official government recall

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