FDA (Drugs) recall action 83788

Pfizer Inc. recalled 2 products on 2019-10-02

The FDA (Drugs) publishes a recall like this one as 2 separate product records. They share a firm, a date and a cause; this page is all of them in one place, so the scale of the action is visible rather than spread across 2 pages.

Products: 2
Announced: 2019-10-02
Critical: 0
Units: —

Why these products were 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.

The agency’s own wording, quoted from the enforcement report.

1–2 of 2

LowFDA (Drugs)··2019-10-02
Pfizer Recalls Ethosuximide Capsules Due to Incorrect Expiration Date Labeling
Pfizer is recalling 7,824 bottles of ethosuximide capsules because the expiration date on the label is incorrect.
Product
ethosuximide capsules, USP, 250 mg, 100-count bottle, Rx Only, Distributed by: Greenstone LLC Peapack, NJ 07977 Made in Netherlands. NDC 59762-2250-2
Category
Distribution
0 states
LowFDA (Drugs)··2019-10-02
Pfizer Recalls Zarontin Capsules Due to Incorrect Expiration Date Labeling
Pfizer is recalling 7,686 bottles of Zarontin (ethosuximide) capsules because the expiration date on the label is incorrect.
Product
ZARONTIN (ETHOSUXIMIDE)
Category
Distribution
0 states

Why these products were recalled

1–2 of 2

Pfizer Recalls Ethosuximide Capsules Due to Incorrect Expiration Date Labeling

Pfizer Recalls Zarontin Capsules Due to Incorrect Expiration Date Labeling