The Recall Desk
SevereFDA (Food)·F-1332-2014·Announced 2014-01-08

Biogenix USA 1 Andro capsules recalled for potential undeclared steroids

Mira Health Products Ltd. is recalling Biogenix USA 1 Andro capsules due to potential contamination with undeclared steroids and pharmaceutical ingredients.

What this means for you

Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.

Our severity reasoning: The agency classified this as an FDA Class II recall. According to the rubric, an FDA Class II recall involving potential contamination with undeclared steroids and pharmaceutical ingredients is categorized as Severe.

Plain-English summary

Mira Health Products Ltd. is recalling Biogenix USA 1 Andro capsules, which are packaged in plastic bottles containing 60 capsules each. The recall is being conducted because the dietary supplements have the potential to be contaminated with undeclared steroids, pharmaceutical ingredients, and/or chemical additives. This risk exists due to a lack of Good Manufacturing Practices (GMPs) during production.

The recall covers all lots of the product that are within their expiry date and were distributed prior to August 2013. The product was distributed in Georgia, Florida, North Carolina, and possibly New Jersey and New Zealand.

Consumers who have purchased these capsules should stop using them and return them to the place of purchase for a refund or contact the recalling firm for further instructions.

The recalled product

Product
Biogenix USA 1 Andro capsules, packaged in plastic bottles with 60 capsules per bottle.

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)

  • All lots within expiry and distributed prior to August 2013

Distribution

Distributed in 3 states:

Part of a larger recall action

This product is one of 79 recalled by Mira Health Products Ltd. under a single FDA (Food) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 79 products in this recall →