Pfizer Inc. recalls Zarontin (ethosuximide capsules, USP) 250 mg, 100-count bottle, Rx Onl,y Made in Netherlands Distributed by Parke-Davis

Recalled October 2, 2019 · FDA recall D-0002-2020 · Pfizer

Hazard

Labeling: Incorrect or Missing Lot and/or Exp Date. The expiry date on the product label is incorrect. The label states an expiry date of 09/2021 when it should be 09/2020. · FDA Class III

Units

7,686 100-count bottles

Sold at

Nationwide in the USA

Description

Labeling: Incorrect or Missing Lot and/or Exp Date. The expiry date on the product label is incorrect. The label states an expiry date of 09/2021 when it should be 09/2020.

Product

Zarontin (ethosuximide capsules, USP) 250 mg, 100-count bottle, Rx Onl,y Made in Netherlands Distributed by Parke-Davis Division of Pfizer In NY, NY 10017, NDC 0071-0237-24

Manufacturer(s)

Pfizer Inc.

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →