The Recall Desk
CriticalFDA (Drugs)·D-0979-2015·Announced 2015-05-13

AMPD GOLD Bee Pollen Recalled for Undeclared Sildenafil

Detox Transforms is recalling AMPD GOLD Bee Pollen capsules because they contain undeclared sildenafil, making them unapproved drugs.

What this means for you

Highest-severity recall. Risk of serious injury or death is documented or strongly suspected. Stop using the product now and follow the agency's instructions.

Our severity reasoning: The agency classification is FDA Class I, which mandates a severity score of 5 according to the rubric.

Plain-English summary

Detox Transforms is recalling 150 bottles of AMPD GOLD Bee Pollen capsules, 350 mg, 60-count. The product was distributed nationwide. The recall covers all lots of the product.

The FDA determined that the product was marketed without an approved New Drug Application (NDA) or Abbreviated New Drug Application (ANDA). The capsules were found to contain undeclared sildenafil, which classifies the product as an unapproved drug.

Consumers who have purchased this product should stop using it and return it to the place of purchase for a refund or contact the recalling firm for instructions.

The recalled product

Product
AMPD GOLD Bee Pollen capsules, 350 mg, 60-count bottle, Signature, 1027 Highway 70 W, Suite 227, Garner, NC 27529, UPC 8 52175 00418 1.
Manufacturer
Detox Transforms
Affected units
150

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (1)

  • Lots: ALL

Distribution

Distributed nationwide across the United States.

Part of a larger recall action

This product is one of 5 recalled by Detox Transforms under a single FDA (Drugs) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 5 products in this recall →