Miraculous Evil Root capsules recall
Miraculous Evil Root capsules, 1200 mg, 6-count bottle, labeling is in foreign language
Why was Miraculous Evil Root capsules recalled?
Marked Without An Approved NDA/ANDA: FDA analysis found these products to contain sildenafil, an FDA approved drug for the treatment of erectile dysfunction, making these products unapproved drugs for which safety and efficacy have not been establish and therefore, subject to recall.
What should I do if I have this product?
Review the official FDA enforcement record for current 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 Lots
- Product
- Miraculous Evil Root capsules, 1200 mg, 6-count bottle, labeling is in foreign language
- Recalling firm
- A&H Focal Inc.
- Quantity
- unknown
- Distribution
- NY and NJ through six retail stores named "Asian Food Markets"
- Recall date
- February 7, 2018
- Classification
- Class I
- Status
- Terminated
- Agency
- FDA (drug)