MegMan Performance Booster recall
MegMan Performance Booster, 800 mg capsules, packaged in 10-count blisters packaged in a carton, UPC 8 48998 00091 2, ASIN B08Z74KS88
Why was MegMan Performance Booster recalled?
Marketed Without An Approved NDA/ANDA: product was found to contain undeclared tadalafil, an ingredient found in FDA approved products for the treatment of male sexual enhancement, making this an unapproved drug.
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?
Lot # 2010291, Exp 01/07/2024
- Product
- MegMan Performance Booster, 800 mg capsules, packaged in 10-count blisters packaged in a carton, UPC 8 48998 00091 2, ASIN B08Z74KS88
- Recalling firm
- Junp Hydration LLC
- Quantity
- 750 cartons
- Distribution
- Product was distributed nationwide in the USA via Amazon Marketplace
- Recall date
- February 16, 2022
- Classification
- Class I
- Status
- Terminated
- Agency
- FDA (drug)