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.
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