# FDA recall D-1443-2014

> **Pfizer Inc.** · Class III · drug recall initiated 2014-07-08.

## Product

VIRACEPT (R) (nelfinavir mesylate) Tablets, 625 mg, 120-count bottle, Rx only, Manufactured by: Agouron Pharmaceuticals, Inc. A Pfizer Company,  Distributed by: ViV Healthcare Company, Research Triangle Park, NC 27709  NDC 63010-027-70

## Reason for recall

Labeling: Incorrect or missing lot and or Exp Date: The bottles were labeled with an incorrect expiry date 11/2016.  The correct expiry date is 09/2016.

## Distribution

Nationwide and Puerto Rico

## Key facts

- **Recall number:** D-1443-2014
- **Recalling firm:** Pfizer Inc.
- **Classification:** Class III
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2014-07-08
- **Report date:** 2014-07-23
- **Termination date:** 2015-07-06

- **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-1443-2014

## Citation

> AI Analytics. FDA recall D-1443-2014. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/D-1443-2014. Source: US FDA. Licensed CC0.

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