Regeneca Recalls RegeneSlim Appetite Control Due to DMAA Presence
Regeneca, Inc. is recalling RegeneSlim Appetite Control dietary supplements because FDA analysis found the product contains DMAA.
The agency’s classification
FDA (Food): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
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 agency classification is FDA Class II, which corresponds to a Severe rating under the rubric, particularly given the presence of DMAA, a substance associated with significant health risks.
Plain-English summary
Regeneca, Inc. is recalling RegeneSlim Appetite Control, 2 capsules/packet, Dietary Supplement. The recall involves 154,748 packets of the product.
The recall was initiated because FDA analysis found that RegeneSlim contains DMAA. The product is sold through multi-level marketing.
Consumers who have purchased RegeneSlim Appetite Control should stop using the product and contact the recalling firm for further instructions.
The recalled product
- Product
- RegeneSlim Appetite Control, 2 capsules/ packet, Dietary Supplement
- Manufacturer
- Regeneca, Inc
- Category
- Food — Dietary Supplement
- Hazard
- Affected units
- 154,748
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 (4)
- 11414RE5516
- EX0616R15814
- 823230415
- EX0616R15813
Distribution
Distribution scope not specified by the agency.
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