US Drug Recall Register

FDA Drug Recalls

1,739 recalls · Class I, newest first

Class I · High risk Terminated

XCEL Capsules

Reason Marketed Without An Approved NDA/ANDA: tainted product marketed as a dietary supplement. Product found to be tainted with undeclared fluoxetine, an FDA approved drug used to treat depression, anxiety, panic attacks, obsessive-compulsive disorder, or bulimia and phenolphthalein, an ingredient found in over-the-counter laxative products that was withdrawn from the US market due to concerns of carcinogenicity, making it an unapproved drug.

Bee Extremely Amazed LLC D-1149-2016
Class I · High risk Terminated

Ultimate Formula Capsules

Reason Marketed Without An Approved NDA/ANDA: tainted product marketed as a dietary supplement. Product found to be tainted with undeclared sibutramine, an appetite suppressant that was withdrawn from the US market for safety reasons, making it an unapproved drug.

Bee Extremely Amazed LLC D-1148-2016
Class I · High risk Terminated

SLIM TRIM U Capsules

Reason Marketed Without An Approved NDA/ANDA: tainted product marketed as a dietary supplement. Product found to be tainted with undeclared sibutramine, an appetite suppressant that was withdrawn from the US market for safety reasons, making it an unapproved drug.

Bee Extremely Amazed LLC D-1147-2016
Class I · High risk Terminated

SlimeX-15 Capsules

Reason Marketed Without An Approved NDA/ANDA: tainted product marketed as a dietary supplement. Product found to be tainted with undeclared sibutramine, an appetite suppressant that was withdrawn from the US market for safety reasons, making it an unapproved drug.

Bee Extremely Amazed LLC D-1146-2016
Class I · High risk Terminated

Prime Capsules

Reason Marketed Without An Approved NDA/ANDA: tainted product marketed as a dietary supplement. Product found to be tainted with undeclared sibutramine, an appetite suppressant that was withdrawn from the US market for safety reasons, and phenolphthalein, an ingredient found in over-the-counter laxative products that was withdrawn from the US market due to concerns of carcinogenicity, making it an unapproved drug.

Bee Extremely Amazed LLC D-1145-2016
Class I · High risk Terminated

Oasis Capsules

Reason Marketed Without An Approved NDA/ANDA: tainted product marketed as a dietary supplement. Product found to be tainted with undeclared sibutramine, an appetite suppressant that was withdrawn from the US market for safety reasons, and phenolphthalein, an ingredient found in over-the-counter laxative products that was withdrawn from the US market due to concerns of carcinogenicity, making it an unapproved drug.

Bee Extremely Amazed LLC D-1144-2016
Class I · High risk Terminated

La' Trim Plus Capsules

Reason Marketed Without An Approved NDA/ANDA: tainted product marketed as a dietary supplement. Product found to be tainted with undeclared sibutramine, an appetite suppressant that was withdrawn from the US market for safety reasons, and phenolphthalein, an ingredient found in over-the-counter laxative products that was withdrawn from the US market due to concerns of carcinogenicity, making it an unapproved drug.

Bee Extremely Amazed LLC D-1143-2016
Class I · High risk Terminated

Jenesis Capsules

Reason Marketed Without An Approved NDA/ANDA: tainted product marketed as a dietary supplement. Product found to be tainted with undeclared sibutramine, an appetite suppressant that was withdrawn from the US market for safety reasons, and phenolphthalein, an ingredient found in over-the-counter laxative products that was withdrawn from the US market due to concerns of carcinogenicity, making it an unapproved drug.

Bee Extremely Amazed LLC D-1142-2016
Class I · High risk Terminated

Infinity Capsules

Reason Marketed Without An Approved NDA/ANDA: tainted product marketed as a dietary supplement. Product found to be tainted with undeclared sibutramine, an appetite suppressant that was withdrawn from the US market for safety reasons, making it an unapproved drug.

Bee Extremely Amazed LLC D-1141-2016
Class I · High risk Terminated

EVOLVE BEE POLLEN Capsules

Reason Marketed Without An Approved NDA/ANDA: tainted product marketed as a dietary supplement. Product found to be tainted with undeclared sibutramine, an appetite suppressant that was withdrawn from the US market for safety reasons, and phenolphthalein, an ingredient found in over-the-counter laxative products that was withdrawn from the US market due to concerns of carcinogenicity, making it an unapproved drug.

Bee Extremely Amazed LLC D-1140-2016
Class I · High risk Terminated

Asset extreme+PLUS Capsules

Reason Marketed Without An Approved NDA/ANDA: tainted product marketed as a dietary supplement. Product found to be tainted with undeclared sibutramine, an appetite suppressant that was withdrawn from the US market for safety reasons, making it an unapproved drug.

Bee Extremely Amazed LLC D-1139-2016
Class I · High risk Terminated

Asset BOLD Capsules

Reason Marketed Without An Approved NDA/ANDA: tainted product marketed as a dietary supplement. Product found to be tainted with undeclared sibutramine, an appetite suppressant that was withdrawn from the US market for safety reasons, and phenolphthalein, an ingredient found in over-the-counter laxative products that was withdrawn from the US market due to concerns of carcinogenicity, making it an unapproved drug.

Bee Extremely Amazed LLC D-1138-2016
Class I · High risk Terminated

Dextrose Injection

Reason Presence of Particulate Matter: Confirmed customer compliants of finding an insect floating in the primary container of each product.

Baxter Healthcare Corp. NDC 0338-0719-06 D-0958-2016
Class I · High risk Terminated

0.9% Sodium Chloride Injection

Reason Presence of Particulate Matter: Confirmed customer compliants of finding an insect floating in the primary container of each product.

Baxter Healthcare Corp. NDC 0338-0049-02 D-0957-2016
Class I · High risk Terminated

Fuel Up High Octane

Reason Marketed Without An Approved NDA/ANDA: Tainted Product Marketed As a Dietary Supplement: Products were found to be tainted with undeclared hydroxythiohomosildenafil, an analogue of Sildenafil, an FDA-approved drug for the treatment of male Erectile Dysfunction (ED), making them unapproved new drugs.

Reesna, Inc D-0960-2016
Class I · High risk Terminated

Fuel Up Plus

Reason Marketed Without An Approved NDA/ANDA: Tainted Product Marketed As a Dietary Supplement: Products were found to be tainted with undeclared hydroxythiohomosildenafil, an analogue of Sildenafil, an FDA-approved drug for the treatment of male Erectile Dysfunction (ED), making them unapproved new drugs.

Reesna, Inc D-0959-2016
Class I · High risk Terminated

Shorts on the Beach capsules

Reason Marketed without an approved NDA/ANDA: Product contains undeclared Sibutramine, Phenolphthalein and/or Diclofenac.

Lucy's Weight Loss (dba. Waisted With Lucy) D-0883-2016
Class I · High risk Terminated

Pink Bikini capsules

Reason Marketed without an approved NDA/ANDA: Product contains undeclared Sibutramine, Phenolphthalein and/or Diclofenac.

Lucy's Weight Loss (dba. Waisted With Lucy) D-0882-2016
Class I · High risk Terminated

LIPO ESCULTURA capsules

Reason Marketed Without An Approved NDA/ANDA: Tainted product marketed as a dietary supplement. Product found to be tainted with sibutramine, an appetite suppressant that was withdrawn from the U.S. market in October 2010 for safety reasons, and diclofenac, a prescription non-steroidal anti-inflammatory drug, making this an unapproved drug.

Lipo Escultura Corp. D-0860-2016
Class I · High risk Terminated

SUPER HERBS 350 mg

Reason Marketed without an approved NDA/ANDA - presence of undeclared sibutramine, desmethylsibutramine (an active metabolite of sibutramine) and/or phenolphthalein.

Super Herbs D-0909-2016
Class I · High risk Ongoing

Vitamin Supplement

Reason Superpotent Drug: The vitamin supplement contains an extremely high level of vitamin D3 (Cholecalciferol).

Glades Drugs Inc. D-0669-2016
Class I · High risk Terminated

Auvi-Q

Reason Defective Delivery System; potential to have inaccurate dosage delivery

Sanofi-Aventis U.S. LLC NDC 0024-5831-02 D-0873-2016
Class I · High risk Terminated

Auvi-Q

Reason Defective Delivery System; potential to have inaccurate dosage delivery

Sanofi-Aventis U.S. LLC NDC 0025-5833-02 D-0872-2016
Class I · High risk Terminated

Natureal Burn Fat Nature

Reason Marketed Without an Approved NDA/ANDA: Product contains undeclared sibutramine.

Inaffit, LLC D-0675-2016
Class I · High risk Terminated

Rhino 7 Platinum 3000

Reason Marketed without an Approved NDA/ANDA: Products contain undeclared active pharmaceutical ingredients; desmethyl carbondenafil and dapoxetine.

MSNV, Inc dba National Video Supply D-0671-2016