Why it was recalled
1 ingredient failed identity testing and 2 ingredients failed microbiological testing (E.coli)
Product description
GnuPharma Sleep 100% Herbal Supplement 60 Capsules
Lot numbers, UPCs & expiration codes
products manufactured prior to May 8th, 2017.
Where it was sold
US
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-0298-2017
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- May 8, 2017
- FDA report date
- Jul 26, 2017
- Quantity
- 1 bottle
- Recall type
- Voluntary: Firm initiated
- Recalling firm
- GnuPharma Corp.
Original FDA data
Every field from FDA enforcement report F-0298-2017, exactly as published.
Show all FDA fields
- City
- Owasso
- State
- OK
- Status
- Terminated
- Country
- United States
- Event ID
- 77506
- Address
- 8751 N 117th East Ave Ste J
- Code information
- products manufactured prior to May 8th, 2017.
- Postal code
- 74055-2098
- Report date
- Jul 26, 2017
- Product type
- Food
- Recall number
- F-0298-2017
- Classification
- Class II
- Recalling firm
- GnuPharma Corp.
- Product quantity
- 1 bottle
- Termination date
- Nov 15, 2018
- Reason for recall
- 1 ingredient failed identity testing and 2 ingredients failed microbiological testing (E.coli)
- Voluntary / mandated
- Voluntary: Firm initiated
- Product description
- GnuPharma Sleep 100% Herbal Supplement 60 Capsules
- Distribution pattern
- US
- Recall initiation date
- May 8, 2017
- Initial firm notification
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Center classification date
- Jul 18, 2017