# FDA recall D-0520-2016

> **Pfizer Inc.** · Class III · drug recall initiated 2015-12-02.

## Product

Norpace CR (disopyramide phosphate) extended-release capsules USP,150 mg, packaged in a) 100-count bottles (NDC 0025-2742-31), and b) 500-count bottles (NDC 0025-2742-51), Rx only, Distributed by G.D. Searle LLC, Division of Pfizer Inc, NY, NY 10017.

## Reason for recall

Failed Dissolution Specification

## Distribution

Nationwide

## Key facts

- **Recall number:** D-0520-2016
- **Recalling firm:** Pfizer Inc.
- **Classification:** Class III
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2015-12-02
- **Report date:** 2015-12-16
- **Termination date:** 2017-07-26

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** New York, NY, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0520-2016

## Citation

> AI Analytics. FDA recall D-0520-2016. Retrieved 2026-05-26 from https://api.ai-analytics.org/recall/D-0520-2016. Source: US FDA. Licensed CC0.

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