PlainRecalls
FDA Drug Low Class III Terminated

ethosuximide capsules, USP, 250 mg, 100-count bottle, Rx Only, Distributed by: Greenstone LLC Peapack, NJ 07977 Made in Netherlands. NDC 59762-2250-2

Reported: October 2, 2019 Initiated: September 12, 2019 #D-0001-2020

Product Description

ethosuximide capsules, USP, 250 mg, 100-count bottle, Rx Only, Distributed by: Greenstone LLC Peapack, NJ 07977 Made in Netherlands. NDC 59762-2250-2

Reason for Recall

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.

Details

Recalling Firm
Pfizer Inc.
Units Affected
7,824 100-count bottles
Distribution
Nationwide in the USA
Location
New York, NY

Frequently Asked Questions

What product was recalled?
ethosuximide capsules, USP, 250 mg, 100-count bottle, Rx Only, Distributed by: Greenstone LLC Peapack, NJ 07977 Made in Netherlands. NDC 59762-2250-2. Recalled by Pfizer Inc.. Units affected: 7,824 100-count bottles.
Why was this product 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.
Which agency issued this recall?
This recall was issued by the FDA Drug on October 2, 2019. Severity: Low. Recall number: D-0001-2020.