Burro en Primavera recall
Burro en Primavera, 2 capsules, UPC 638632431055
Why was Burro en Primavera recalled?
Marketed without Approved NDA/ANDA: FDA analysis results obtained the presence of tadalafil and/or sildenafil.
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
All
- Product
- Burro en Primavera, 2 capsules, UPC 638632431055
- Recalling firm
- QMart
- Quantity
- 500 boxes
- Distribution
- USA Nationwide
- Recall date
- May 12, 2021
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (drug)