GM Manufacturing Recalls Ninja Mojo Dietary Supplements for cGMP Violations
GM Manufacturing is recalling Ninja Mojo dietary supplements due to significant violations of current Good Manufacturing Practice (cGMP) regulations.
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 2/5 (Moderate).
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: The recall is classified as FDA Class II, which typically involves a situation where use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences. The source cites cGMP violations without reporting specific illnesses or injuries, aligning with a Moderate severity rating.
Plain-English summary
GM Manufacturing Inc. is voluntarily recalling Ninja Mojo, small vinyl Packs, dietary supplements. The recall is being conducted due to significant violations of the current Good Manufacturing Practice (cGMP) regulations for dietary supplements.
Approximately 50,000 units of the product were distributed in California. The affected product is identified by the lot code LOT08152013 and has an expiration date of December 2016.
Consumers who have purchased this product should stop using it and contact GM Manufacturing Inc. for further instructions or a refund.
The recalled product
- Product
- Ninja Mojo, small vinyl Packs
- Manufacturer
- GM Manufacturing Inc.
- Category
- Drug — Dietary Supplements
- Hazard
- Affected units
- 50,000
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)
- LOT08152013 EXPDEC2016
Distribution
Distributed in 1 state:
Part of a larger recall action
This product is one of 46 recalled by GM Manufacturing 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.
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