Pfizer Inc. recalls quinapril HCl/hydrochlorothiazide tablets, 20 mg/12.5 mg*, 9
See all recalls from Pfizer Inc. →Recalled Product
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
Hazard / Issue
CGMP Deviations: N-nitroso-quinapril and N-nitroso-hydrochlorothiazide impurity above the acceptable daily intake limit.
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: Lots DN6931, ED3904 & ED3905; Exp. 03/2023
✅ What Should You Do?
- 1Stop taking this medication and contact your doctor or pharmacist immediately.
- 2Do NOT flush medications down the drain — use an FDA-approved drug take-back program.
- 3Check the lot number on your bottle or packaging against the recalled lots listed above.
- 4Report adverse events to FDA MedWatch or call 1-800-FDA-1088.
Looking for a safe alternative?
Search Amazon for quinapril HCl/hydrochlorothiazide tablets, 20 →If you were harmed by this recalled product, Top Class Actions lists active class action lawsuits and settlements that may apply to you.
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