Why it was recalled
Product is sub-potent for Vitamin D and label contains incorrect percent daily value.
Product description
Healthprint Vitamin D3 5000 Dietary Supplement, 200 tablets, packaged in plastic bottle.
Lot numbers, UPCs & expiration codes
Lot 063-0723
Where it was sold
FL
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-0930-2024
- Classification
- Class III
- Status
- Terminated
- Recall initiated
- Jan 25, 2024
- FDA report date
- Mar 6, 2024
- Quantity
- 111 bottles
- Recall type
- Voluntary: Firm initiated
- Recalling firm
- Ancient Formulas, Inc.
Original FDA data
Every field from FDA enforcement report F-0930-2024, exactly as published.
Show all FDA fields
- City
- Wichita
- State
- KS
- Status
- Terminated
- Country
- United States
- Event ID
- 93899
- Address
- 1235 S Santa Fe St
- Code information
- Lot 063-0723
- Postal code
- 67211-3223
- Report date
- Mar 6, 2024
- Product type
- Food
- Recall number
- F-0930-2024
- Classification
- Class III
- Recalling firm
- Ancient Formulas, Inc.
- Product quantity
- 111 bottles
- Termination date
- Feb 29, 2024
- Reason for recall
- Product is sub-potent for Vitamin D and label contains incorrect percent daily value.
- Voluntary / mandated
- Voluntary: Firm initiated
- Product description
- Healthprint Vitamin D3 5000 Dietary Supplement, 200 tablets, packaged in plastic bottle.
- Distribution pattern
- FL
- Recall initiation date
- Jan 25, 2024
- Initial firm notification
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Center classification date
- Feb 26, 2024