Why it was recalled
FDA sample analysis of Biotin 1000mg Lot #1345 showed the product Biotin content to be 0.8% of label claim.
Product description
Biotin 1000mcg, Dietary Supplement, 30 Tablets, Manufactured by: Golden Nutrition
Lot numbers, UPCs & expiration codes
Lot #1345 EXP 09/22
Where it was sold
Domestic distribution only.
What to do if you have this product
- Compare the brand, size, and lot/UPC codes on your package with the codes above.
- If it matches, don't eat it. Return it to the store for a refund or throw it away.
- Wash surfaces and containers that touched the product.
- If you feel sick after eating it, contact your doctor. In an emergency call 911.
Recall details
- Recall number
- F-0930-2020
- Classification
- Class III
- Status
- Terminated
- Recall initiated
- Apr 6, 2020
- FDA report date
- May 6, 2020
- Quantity
- 120 bottles
- Recall type
- Voluntary: Firm initiated
- Recalling firm
- GOLDEN NUTRITION INC
Original FDA data
Every field from FDA enforcement report F-0930-2020, exactly as published.
Show all FDA fields
- City
- Opa Locka
- State
- FL
- Status
- Terminated
- Country
- United States
- Event ID
- 85496
- Address
- 13461 Nw 47th Ave
- Code information
- Lot #1345 EXP 09/22
- Postal code
- 33054-4317
- Report date
- May 6, 2020
- Product type
- Food
- Recall number
- F-0930-2020
- Classification
- Class III
- Recalling firm
- GOLDEN NUTRITION INC
- Product quantity
- 120 bottles
- Termination date
- Aug 21, 2020
- Reason for recall
- FDA sample analysis of Biotin 1000mg Lot #1345 showed the product Biotin content to be 0.8% of label claim.
- Voluntary / mandated
- Voluntary: Firm initiated
- Product description
- Biotin 1000mcg, Dietary Supplement, 30 Tablets, Manufactured by: Golden Nutrition
- Distribution pattern
- Domestic distribution only.
- Recall initiation date
- Apr 6, 2020
- Initial firm notification
- Center classification date
- Apr 29, 2020