Testosterzone dietary supplement recalled for undeclared milk allergen
Progressive Laboratories is recalling Testosterzone dietary supplements because they may contain undeclared milk, a major food allergen.
The agency’s classification
FDA (Food): Class I
Class I is a situation in which there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or death.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 4/5 (Severe).
The hazard poses a serious risk of illness, injury, or structural failure. Stop using the product immediately and contact the manufacturer for a refund or repair.
Our severity reasoning: The recall is classified as FDA Class I, which meets the rubric criteria for a score of 4 (Severe) as it indicates a reasonable probability of serious adverse health consequences.
Plain-English summary
Progressive Laboratories, Inc. is recalling 669 bottles of Testosterzone dietary supplements. The product is packaged in an amber plastic bottle with a black cap and contains 180 units per bottle. The recall is due to the potential presence of undeclared milk, which is a major food allergen.
The affected product is identified by Lot # 2072237. It was distributed nationwide through the United States. The U.S. Food and Drug Administration has classified this recall as Class I, indicating a reasonable probability that use of the product will cause serious adverse health consequences or death.
Consumers with this product should stop using it immediately and contact Progressive Laboratories, Inc. for instructions on how to return the product or obtain a refund. Individuals with a milk allergy or sensitivity should be particularly cautious and avoid using the recalled product.
The recalled product
- Product
- Testosterzone 180 count bottle packaged in an amber plastic bottle with a black cap
- Manufacturer
- Progressive Laboratories, Inc
- Category
- Food — Dietary Supplement
- Affected units
- 669
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)
- Lot # 2072237
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 4 recalled by Progressive Laboratories, Inc 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 4 products in this recall →Related recalls
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