GM Manufacturing Recalls CKLS Capsules for cGMP Violations
GM Manufacturing is recalling CKLS capsules due to significant violations of current Good Manufacturing Practice (cGMP) regulations for dietary supplements.
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 situation where use of, or exposure to, a violative product may cause temporary or medically reversible 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 recalling CKLS, Capsules, a dietary supplement product. The recall was initiated because the product was found to have significant violations of the current Good Manufacturing Practice (cGMP) regulations specifically applicable to dietary supplements.
The recall involves 1,000,500 units of the product. The distribution pattern is listed as CA, indicating the product was distributed in California. No specific lot numbers are provided in the recall notice.
Consumers who have purchased CKLS capsules should stop using the product and contact GM Manufacturing Inc. for further instructions or a refund, as per standard recall procedures.
The recalled product
- Product
- CKLS, Capsules
- Manufacturer
- GM Manufacturing Inc.
- Category
- Food — Dietary Supplement
- Hazard
- Affected units
- 1,000,500
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)
- No Lot numbers
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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