F-0747-2014 Class II Terminated
FDA food recall F-0747-2014 was initiated by National Enzyme Co on Oct 30, 2013 and is designated Class II. Reason for recall: Firm is recalling dietary supplements containing a raw material which may contain >0.3 ppb chloramphenicol The recall status is terminated (terminated Mar 3, 2015). Affected quantity: 16733 bottles.
Recall Details
- Product Type
- Food
- Report Date
- Dec 25, 2013
- Initiation Date
- Oct 30, 2013
- Termination Date
- Mar 3, 2015
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 16733 bottles
Product Description
Dietary Supplement packaged in the following configurations: (1) KIRKMAN, Enzym-Complete / DPP-IV, Broad Spectrum Digestion Formula with Dipeptidyl Peptidase IV Analog, packaged in 60-capsule bottles (SKU 52587), 120-capsule bottles (SKU 52588), and 200-capsule bottles (SKU 53853). Manufactured exclusively for KIRKMAN, Lake Oswego, OR; (2) KIRKMAN, EnZym-Complete / DPP-IV, GF/CF Enzyme Dietary Supplement, packaged in 200-capsule bottles (SKU 54956). Manufactured exclusively for KIRKMAN, Lake Oswego, OR;
Reason for Recall
Firm is recalling dietary supplements containing a raw material which may contain >0.3 ppb chloramphenicol
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.
Code Information
Lot #'s: 52587047, 52587048, 52587049, 52587050, 52588047, 52588048, 52588049, 52588050, 52588051, 53853006, 53853007, 53853008, 53853009, 53853010, and 54956000
Source
- Dataset
- openFDA food recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for F-0747-2014
- openFDA file date
- Oct 23, 2026
- Loaded by RegDataLab
- Oct 23, 2026