Recall archive / FDA food enforcement
Pharma Natural, Biotin 5000 mcg, Maximum Strength, Dietary Supplement, 30 Tablets — FDA record F-1615-2023
Reported terminated
Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.
Source date Aug 15, 2023. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.
Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.
What the record says
- Product
- Pharma Natural, Biotin 5000 mcg, Maximum Strength, Dietary Supplement, 30 Tablets
- Reason
- FDA sample analysis of Pharma Natural Biotin 5000 mcg Maximum Strength (30 tablets, Lot: PN10686, Exp. Date 01/24), found the biotin content was below the detection limit.
- Classification
- Class III
- Recalling firm
- Pharma-Natural Inc.
- Quantity
- 204 bottles (102 twin packs)/30 tablets per bottle
- Agency-reported status
- Terminated
- Source record identifier
- F-1615-2023
What the recall classes mean. Classification is an agency assessment, not individual medical advice.
Lot and product identifiers
| Label field | Details supplied by the agency |
|---|---|
| Lot, code or applicability | Lot: PN10686, Exp. Date 01/24 |
Match all identifying details in the current notice. A brand name alone is not enough.
Distribution
Puerto Rico
No US distribution state could be established from this record. Check the official notice.
Dates in the source
- Report date
- Oct 4, 2023
- Recall initiation date
- Aug 15, 2023
- Center classification date
- Sep 27, 2023
- Termination date
- Jan 19, 2024
FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.