RECALL ALERT
Terminated
XLSX-1C7C725C39
Pfizer: Accupril (Quinapril HCl) tablets 10mg, 20mg, 40 mg
Recalled by Pfizer
Classification
—
Reason for Recall
Due to N-Nitroso-Quinapril Content
Product Details
Product Quantity
Not specified
Product Type
Food
Code Info
Not specified
Voluntary/Mandated
Not specified
Distribution & Geography
Distribution Pattern
Not specified
Company Location
Not specified
Timeline
Report Date
04/22/2022
Recall Initiated
04/22/2022
Classification Date
N/A
Termination Date
N/A
Source: U.S. Food & Drug Administration (FDA) — FDA Recalls
Last updated: August 29, 2026
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