GM Manufacturing Recalls DMSA Dietary Supplements for cGMP Violations
GM Manufacturing is recalling 414 units of DMSA dietary supplements due to significant violations of current Good Manufacturing Practice (cGMP) 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 and involves cGMP violations without reported illnesses or specific acute hazards like allergens or pathogens, fitting the criteria for moderate severity.
Plain-English summary
GM Manufacturing Inc. is voluntarily recalling 414 units of DMSA dietary supplements, packaged in 100cc HDPE bottles. The recall is being conducted due to significant violations of the current Good Manufacturing Practice (cGMP) regulations for dietary supplements.
The affected product is identified by lot number LOTKZ8010 and has an expiration date of 10.2016. The recall is limited to distribution in California (CA).
Consumers who have purchased this product should stop using it and contact the manufacturer for further instructions or a refund.
The recalled product
- Product
- DMSA, 100cc HDPE bottle
- Manufacturer
- GM Manufacturing Inc.
- Category
- Food — Dietary Supplements
- Hazard
- Affected units
- 414
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)
- LOTKZ8010 EXP10.2016
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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