Golden Nutrition Recalls Biotin Supplement Due to Low Content
Golden Nutrition is recalling Biotin 1000mcg tablets because FDA testing found the biotin content was only 0.8% of the label claim.
What this means for you
Cosmetic or documentation issue. No expected health impact, but the manufacturer is correcting the affected products.
Our severity reasoning: The recall is classified as FDA Class III, which is defined as unlikely to cause adverse health consequences. The issue is a labeling/quality discrepancy regarding ingredient content rather than a safety hazard like contamination or injury risk.
Plain-English summary
Golden Nutrition Inc. is recalling 120 bottles of Biotin 1000mcg, Dietary Supplement, 30 Tablets. The product was distributed domestically. The recall involves Lot #1345 with an expiration date of 09/22.
The recall was initiated after FDA sample analysis showed that the biotin content in the product was only 0.8% of the label claim. This indicates the product does not contain the amount of biotin stated on the label.
Consumers who purchased this product should stop using it and return it to the place of purchase for a refund or contact the recalling firm for further instructions.
The recalled product
- Product
- Biotin 1000mcg, Dietary Supplement, 30 Tablets, Manufactured by: Golden Nutrition
- Manufacturer
- GOLDEN NUTRITION INC
- Category
- Food — Dietary Supplement
- Hazard
- Affected units
- 120
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)
- Lot #1345 EXP 09/22
Distribution
Distribution scope not specified by the agency.
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