Why it was recalled
Firm is recalling dietary supplements containing a raw material which may contain >0.3 ppb chloramphenicol
Product description
B911 Kirkman Max Spectrum E, packaged unlabeled, 90-capsule bottles (SKU 54255);
Lot numbers, UPCs & expiration codes
Lot #: 54255000
Where it was sold
Domestic distribution of the product is nationwide with direct accounts in 27 states in all geographical regions. Foreign distribution consists of direct accounts in the following countries: Canada, China, Malaysia, Norway, Slovakia, South Korea, Sweden, Taiwan, and the United Kingdom.
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-0792-2014
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- Oct 30, 2013
- FDA report date
- Dec 25, 2013
- Quantity
- 1138 bottles
- Recall type
- Voluntary: Firm initiated
- Recalling firm
- National Enzyme Co
Original FDA data
Every field from FDA enforcement report F-0792-2014, exactly as published.
Show all FDA fields
- City
- Forsyth
- State
- MO
- Status
- Terminated
- Country
- United States
- Event ID
- 66658
- Address
- 10203 State Highway 76
- Code information
- Lot #: 54255000
- Postal code
- 65653-5445
- Report date
- Dec 25, 2013
- Product type
- Food
- Recall number
- F-0792-2014
- Classification
- Class II
- Recalling firm
- National Enzyme Co
- Product quantity
- 1138 bottles
- Termination date
- Mar 3, 2015
- Reason for recall
- Firm is recalling dietary supplements containing a raw material which may contain >0.3 ppb chloramphenicol
- Voluntary / mandated
- Voluntary: Firm initiated
- Product description
- B911 Kirkman Max Spectrum E, packaged unlabeled, 90-capsule bottles (SKU 54255);
- Distribution pattern
- Domestic distribution of the product is nationwide with direct accounts in 27 states in all geographical regions. Foreign distribution consists of direct accounts in the following countries: Canada, China, Malaysia, Norway, Slovakia, South Korea, Sweden, Taiwan, and the United Kingdom.
- Recall initiation date
- Oct 30, 2013
- Initial firm notification
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Center classification date
- Dec 13, 2013