Home / Triceutical Inc./Zhang / F-0108-2017
Class III
Triceutical Inc./Zhang
Recall #F-0108-2017 · Initiated 2014-10-10
Plain-language summary
by FoodRecallsDB.infoWhat happened
Triceutical Inc. recalled all bottles of CardioAdvance dietary supplements because the company did not follow FDA manufacturing safety standards. A total of 528 bottles were distributed in Florida, New York, Pennsylvania, and China.
Who is at risk
Anyone who purchased CardioAdvance should be aware of this recall, though the risk is considered low (Class III classification).
What to do
Check if you have CardioAdvance at home and stop using it. Contact the manufacturer or your retailer for instructions on returning the product or obtaining a refund.
Product
CardioAdvance
Reason for recall
Triceutical Inc. has recalled all dietary supplements due to lack of good manufacturing practices.
Quantity affected
528 bottles
Distribution
*Domestic* - FL, NY, PA, *International*- China
Lot / code info
all lot numbers, all expiration dates
Voluntary / mandated
Voluntary: Firm initiated
Initial notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Terminated
2018-06-04
Recalling firm
Triceutical Inc./Zhang
164 Milbar Blvd
Farmingdale, NY 11735-1425
United States
Recall classification
Unlikely to cause any adverse health consequences.