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

Recall date

September 12, 2019

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

D-0002-2020

FDA classification

Class III

Brand / firm

Pfizer Inc.

Sold / distributed

Nationwide in the USA

Why it was recalled

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.

Class III means the product violates regulations but is not likely to cause harm.

What was recalled

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