Severity
Low
FDA Food recall · Reported May 6, 2020
FDA sample analysis of Biotin 1000mg Lot #1345 showed the product Biotin content to be 0.8% of label claim.
Golden Nutrition INC recalled Biotin 1000mcg, Dietary Supplement, 30 Tablets, Manufactured by: Golden Nutrition - a low-severity action.
Biotin 1000mcg, Dietary Supplement, 30 Tablets, Manufactured by: Golden Nutrition was recalled by Golden Nutrition INC in May 6, 2020. Reason: FDA sample analysis of Biotin 1000mg Lot #1345 showed the product Biotin content to be 0.8% of label claim.. Check the official notice for the remedy. Verify recall #F-0930-2020 with the FDA Food before acting.
The recall
Golden Nutrition INC issued this low-severity FDA Food recall-FDA sample analysis of Biotin 1000mg Lot #1345 showed the product Biotin content to be 0.8% of label claim..
Sourced from official FDA Food enforcement records. Verify recall #F-0930-2020 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
This FDA Food action (record #F-0930-2020) was formally reported on May 6, 2020, with the manufacturer initiating the action on April 6, 2020. It is classified under Low severity (Class III), with a current status of Terminated. Golden Nutrition INC is listed as the recalling firm, operating out of Opa Locka, FL. Federal records list the affected scope as 120 bottles.
The documented reason for this recall is: FDA sample analysis of Biotin 1000mg Lot #1345 showed the product Biotin content to be 0.8% of label claim. Distribution data in the federal record shows the product reached: Domestic distribution only.. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 6 from FDA Food - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Where this recall sits in its category - 2,002 dietary supplements recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified low severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Severity
Low
Affected scope
120 bottles
Related Recalls
6
6 from same agency
Biotin 1000mcg, Dietary Supplement, 30 Tablets, Manufactured by: Golden Nutrition
FDA sample analysis of Biotin 1000mg Lot #1345 showed the product Biotin content to be 0.8% of label claim.
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Low (Class III) |
| Status | Terminated |
| Recall number | F-0930-2020 |
| Date reported | May 6, 2020 |
| Date initiated | April 6, 2020 |
| Recalling firm | Golden Nutrition INC |
| Firm location | Opa Locka, FL |
| Affected scope | 120 bottles |
| Distribution | Domestic distribution only. |
Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
This page summarizes the official FDA Food record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Food, reported May 6, 2020. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.