Drug & medication recalls Moderate risk

QMart recalls Burro en Primavera, 2 capsules, UPC 638632431055

Recall date
March 31, 2021
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
D-0370-2021
FDA classification
Class II
Brand / firm
QMart
Sold / distributed
USA Nationwide

Why it was recalled

Marketed without Approved NDA/ANDA: FDA analysis results obtained the presence of tadalafil and/or sildenafil.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

Burro en Primavera, 2 capsules, UPC 638632431055

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