Mira Health Recalls Nature Science 1 Andro Capsules Due to Steroid Contamination Risk
Mira Health Products Ltd. is recalling Nature Science 1 Andro capsules because they may contain undeclared steroids or chemical additives due to poor manufacturing practices.
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 recall is classified as FDA Class II, and the rubric specifies that FDA Class II recalls involving significant risks such as undeclared steroids or pharmaceutical ingredients are categorized as Severe.
Plain-English summary
Mira Health Products Ltd. is recalling Nature Science 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 affected products are all lots that were within their expiry date and distributed prior to August 2013. The supplements were distributed in Georgia, Florida, North Carolina, and possibly New Jersey and New Zealand.
Consumers who have purchased these products should stop using them immediately. They should contact the recalling firm for further instructions or return the product to the place of purchase.
The recalled product
- Product
- Nature Science 1 Andro capsules packaged in a plastic bottle with 60 capsules per bottle.
- Manufacturer
- Mira Health Products Ltd.
- Category
- Food — Dietary Supplement
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
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.
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