GM Manufacturing Recalls Albert Capsules for cGMP Violations
GM Manufacturing is recalling Albert Capsules 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, which typically corresponds to a moderate severity level involving temporary or medically reversible adverse health consequences, without reported serious injuries or deaths.
Plain-English summary
GM Manufacturing Inc. is recalling Albert 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 for dietary supplements.
The recall involves 81,600 units of the product. Distribution was limited to California. The source text does not specify specific lot numbers or expiration dates, but the structured data indicates production dates ranging from March 2012 to November 2012.
Consumers who have purchased Albert Capsules should stop using the product and contact GM Manufacturing Inc. for further instructions or a refund. The recall is classified as Class II by the FDA, indicating that there is a reasonable probability that the use of or exposure to the violative product may cause temporary or medically reversible adverse health consequences.
The recalled product
- Product
- Albert, Capsules
- Manufacturer
- GM Manufacturing Inc.
- Category
- Food — Dietary Supplement
- Hazard
- Affected units
- 81,600
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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