FDA recall record
Biofilm Defense, Kirkman brand, Item # 0881-060 and 5881-060 Biofilm Defense, Pure Compounding brand, Item # 1881-060.
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
Biofilm Defense, Kirkman brand, Item # 0881-060 and 5881-060 Biofilm Defense, Pure Compounding brand, Item # 1881-060.
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.
Biofilm Defense, Kirkman brand, Item # 0881-060 and 5881-060 Biofilm Defense, Pure Compounding brand, Item # 1881-060.
Code information listed by FDA
LOT numbers: 53666006, 53666007, 53666008, 53666009,
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: 6099 bottles (5489 bottles in US and 610 outside the 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.