Xzen Platinum recall
XZEN PLATINUM, 750 mg, Distributed by: XZEN, Los Angeles, CA.
Why was Xzen Platinum recalled?
Marketed Without an Approved NDA/ANDA: These dietary supplements contain undeclared sildenafil, an analogue of sildenafil, and/or tadalafil.
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 130520PL Exp. 05/31/2017
- Product
- XZEN PLATINUM, 750 mg, Distributed by: XZEN, Los Angeles, CA.
- Recalling firm
- Schindele Enterprises dba Midwest Wholesale
- Quantity
- 89 blister packs
- Distribution
- Distributed to PA, IL, TX, IA, GA, CT, FL, CA, LA, NY, MD, NV, and WI
- Recall date
- May 28, 2014
- Classification
- Class I
- Status
- Terminated
- Agency
- FDA (drug)