PlainRecalls
FDA Drug Critical Class I Terminated

Oasis Dietary Supplement Capsules, 500 mg, 45 count bottles, Manufactured for Timeless Solutions, 1810 E Sahara Ave #100, Las Vegas, Nevada 89104, distributed by BeeXtreme LLC, Punxsutawney PA

Reported: October 19, 2016 Initiated: December 23, 2015 #D-0020-2017

Product Description

Oasis Dietary Supplement Capsules, 500 mg, 45 count bottles, Manufactured for Timeless Solutions, 1810 E Sahara Ave #100, Las Vegas, Nevada 89104, distributed by BeeXtreme LLC, Punxsutawney PA

Reason for Recall

Marketed without an Approved NDA/ANDA; FDA analysis found them to contain sibutramine and phenolphthalein

Details

Recalling Firm
Bee Xtreme
Units Affected
732 bottles
Distribution
Unknown
Location
Punxsutawney, PA

Frequently Asked Questions

What product was recalled?
Oasis Dietary Supplement Capsules, 500 mg, 45 count bottles, Manufactured for Timeless Solutions, 1810 E Sahara Ave #100, Las Vegas, Nevada 89104, distributed by BeeXtreme LLC, Punxsutawney PA. Recalled by Bee Xtreme. Units affected: 732 bottles.
Why was this product recalled?
Marketed without an Approved NDA/ANDA; FDA analysis found them to contain sibutramine and phenolphthalein
Which agency issued this recall?
This recall was issued by the FDA Drug on October 19, 2016. Severity: Critical. Recall number: D-0020-2017.