Why it was recalled
Marketed without an Approved NDA/ANDA; FDA analysis found them to contain sibutramine and phenolphthalein
Product description
La' Trim Plus 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
Lot numbers, UPCs & expiration codes
All Lots
Where it was sold
Unknown
What to do if you have this product
- Compare the lot number and expiration date on your package with the codes above.
- Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
- If you have symptoms you think are related, contact your doctor. In an emergency call 911.
- Report side effects to FDA MedWatch at 1-800-FDA-1088.
Recall details
- Recall number
- D-0019-2017
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- Dec 23, 2015
- FDA report date
- Oct 19, 2016
- Quantity
- 589 bottles
- Recall type
- Voluntary: Firm initiated
- Recalling firm
- Bee Xtreme
Original FDA data
Every field from FDA enforcement report D-0019-2017, exactly as published.
Show all FDA fields
- City
- Punxsutawney
- State
- PA
- Status
- Terminated
- Country
- United States
- Event ID
- 73167
- Address
- 506 N Penn St
- Code information
- All Lots
- Postal code
- 15767-1527
- Report date
- Oct 19, 2016
- Product type
- Drugs
- Recall number
- D-0019-2017
- Classification
- Class I
- Recalling firm
- Bee Xtreme
- Product quantity
- 589 bottles
- Termination date
- Jan 30, 2017
- Reason for recall
- Marketed without an Approved NDA/ANDA; FDA analysis found them to contain sibutramine and phenolphthalein
- Voluntary / mandated
- Voluntary: Firm initiated
- Product description
- La' Trim Plus 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
- Distribution pattern
- Unknown
- Recall initiation date
- Dec 23, 2015
- Initial firm notification
- Center classification date
- Oct 12, 2016