# FDA recall D-1556-2014

> **Alkermes, Inc.** · Class II · drug recall initiated 2014-03-04.

## 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.

## Reason for recall

Customer complaints for failure to deliver the dose.

## Distribution

Nationwide

## Key facts

- **Recall number:** D-1556-2014
- **Recalling firm:** Alkermes, Inc.
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2014-03-04
- **Report date:** 2014-09-03
- **Termination date:** 2014-12-22

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Waltham, MA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1556-2014

## Citation

> AI Analytics. FDA recall D-1556-2014. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/D-1556-2014. Source: US FDA. Licensed CC0.

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