FDAFDA · Food and drugs·Recall number D-0759-2022
quinapril HCl/hydrochlorothiazide tablets, 20 mg/12.5 mg*, 90 Tablets bottles, Rx Only, Distributed by: Greenstone, LLC, Peapack, NJ, 07977, Made in Germany, NDC 59762-0220-1
Published April 13, 2022 · Recall initiated: March 21, 2022
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
CGMP Deviations: N-nitroso-quinapril and N-nitroso-hydrochlorothiazide impurity above the acceptable daily intake limit.
What to do
Voluntary: Firm initiated · Press Release
Recall details
- Manufacturer
- Pfizer Inc.
- Distributor
- Nationwide
- Lot
- Lots DN6931, ED3904 & ED3905; Exp. 03/2023
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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