FDA recall record
EnZym-Complete/DPP-IV II with Isogest, Kirkman brand. Item numbers: 0851A-090, 0851A-180, 0931-090, 0931-180, 5851A-090, 5931-090.
FDA classification. FDA Class I, II, and III are not the same as USDA FSIS classifications and are not a cross-agency safety score.
FDA listed a termination date of April 2, 2014. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
EnZym-Complete/DPP-IV II with Isogest, Kirkman brand. Item numbers: 0851A-090, 0851A-180, 0931-090, 0931-180, 5851A-090, 5931-090.
Reason
Firm is recalling dietary supplements containing a raw material which may contain >0.3 ppb chloramphenicol
Products involved
Product descriptions are copied from the FDA recall record. They are not a current catalog and are not automatically matched to WhoMadeMyFood product pages.
EnZym-Complete/DPP-IV II with Isogest, Kirkman brand. Item numbers: 0851A-090, 0851A-180, 0931-090, 0931-180, 5851A-090, 5931-090.
Code information listed by FDA
Lot numbers: 52939039, 52939040, 52939042, 52939043, 53852011, 53852012, 53852013, 53852015, 53852016,
Distribution and firm information
Recalling firm listed by FDA: Kirkman Group Inc.
Firm location listed by FDA: Lake Oswego, OR, United States
Distribution reported by FDA: distributed worldwide
Product quantity listed by FDA: 9486 bottles (5584 bottles in the US and 3902 bottles outside US)
Source
Source: U.S. Food and Drug Administration (FDA), openFDA food enforcement reports.
Official FDA openFDA food enforcement record
Identifying an FDA recall record does not imply FDA endorsement of WhoMadeMyFood. Methodology.