Burro en Primavera, 2 capsules, UPC 638632431055
Reported: May 12, 2021 Initiated: March 31, 2021 #D-0370-2021
Product Description
Burro en Primavera, 2 capsules, UPC 638632431055
Reason for Recall
Marketed without Approved NDA/ANDA: FDA analysis results obtained the presence of tadalafil and/or sildenafil.
Details
- Recalling Firm
- QMart
- Units Affected
- 500 boxes
- Distribution
- USA Nationwide
- Location
- Elmwood Park, NJ
Frequently Asked Questions
What product was recalled? ▼
Burro en Primavera, 2 capsules, UPC 638632431055. Recalled by QMart. Units affected: 500 boxes.
Why was this product recalled? ▼
Marketed without Approved NDA/ANDA: FDA analysis results obtained the presence of tadalafil and/or sildenafil.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on May 12, 2021. Severity: Moderate. Recall number: D-0370-2021.
Related Recalls
FDA Drug Moderate
Bisoprolol Fumarate and Hydrochlorothiazide tablets, USP, 2.5 mg/6.25 mg, 100-count bottle, Rx Only, Manufactured by: U…
Unichem Pharmaceuticals USA Inc. · 2026-02-11
FDA Drug Critical
Green Lumber Natural Fuel For Men capsule, packaged in 2, 4, 10, and 30-count blister packs. GreenLumber.com, 2618 San…
Green Lumber Holdings, LLC · 2026-02-11
FDA Drug Moderate
Trazodone Hydrochloride, USP, 50 mg, 100-Count Bottle, Rx only, Manufactured by: Granules India Limited, Hyderabad, 500…
Granules Pharmaceuticals Inc. · 2026-02-11
FDA Drug Critical
Diclofenac Sodium, Topical Gel, 3%, 100 g, Rx only, Mfd. by: Taro Pharmaceuticals Inc., Brampton, Ontario, Canada L6T 1…
SUN PHARMACEUTICAL INDUSTRIES INC · 2026-02-11
FDA Drug Critical
Rheumacare capsules, 30 count bottle, Mfg in India by: Virgo UAP Pharma Pvt. Ltd., Ahmedabad, India UPC 8 904218 700313
HANDELNINE GLOBAL LLC · 2026-02-11