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
Reported: October 2, 2019 Initiated: September 12, 2019 #D-0002-2020
Product Description
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
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
- 7,686 100-count bottles
- Distribution
- Nationwide in the USA
- Location
- New York, NY
Frequently Asked Questions
What product 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. Recalled by Pfizer Inc.. Units affected: 7,686 100-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-0002-2020.
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