Jenesis Dietary Supplement Capsules recall
Jenesis Dietary Supplement Capsules, 350 mg, 60 count bottles, Manufactured for Timeless Solutions, 1810 E Sahara Ave #100, Las Vegas, Nevada 89104, distributed by BeeXtreme LLC, Punxsutawney PA
Why was Jenesis Dietary Supplement Capsules recalled?
Marketed without an Approved NDA/ANDA; FDA analysis found them to contain sibutramine and phenolphthalein
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
- Jenesis Dietary Supplement Capsules, 350 mg, 60 count bottles, Manufactured for Timeless Solutions, 1810 E Sahara Ave #100, Las Vegas, Nevada 89104, distributed by BeeXtreme LLC, Punxsutawney PA
- Recalling firm
- Bee Xtreme
- Quantity
- 13 bottles
- Distribution
- Unknown
- Recall date
- October 19, 2016
- Classification
- Class I
- Status
- Terminated
- Agency
- FDA (drug)