GM Manufacturing Recalls Maxium and Prolong Dietary Supplements
GM Manufacturing is recalling Maxium and Prolong capsules due to significant violations of dietary supplement manufacturing regulations.
What this means for you
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 reasonable probability of temporary or medically reversible health consequences. The source cites significant cGMP violations but does not report specific illnesses, injuries, or high-risk pathogens, aligning with a Moderate severity rating.
Plain-English summary
GM Manufacturing Inc. is recalling 62,280 units of Maxium, Capsules and Prolong, Capsules. The recall is being conducted because the products were found to have significant violations of the current Good Manufacturing Practice (cGMP) regulations for dietary supplements.
The affected products were distributed in California (CA). The source text does not specify specific lot numbers, expiration dates, or other identifying codes beyond the general product names and manufacturer.
Consumers who have purchased these products should stop using them and contact GM Manufacturing Inc. for further instructions or a refund.
The recalled product
- Product
- Maxium, Capsules; Prolong, Capsules
- Manufacturer
- GM Manufacturing Inc.
- Category
- Food — Dietary Supplements
- Hazard
- Affected units
- 62,280
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)
- 11/1/13 > 11/15/13
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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