FDA recall record
Formula KB packaged in 1 FL OZ (29mL) droppers. HoneyCombs Industries, 10671 6075 Road, Montrose, CO 81403.
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 March 2, 2017. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
Formula KB packaged in 1 FL OZ (29mL) droppers. HoneyCombs Industries, 10671 6075 Road, Montrose, CO 81403.
Reason
The powdered golden seal had a coliform count of 2000 cfu/g when the specifications stated less than 1000/cfy/g. There is 12mg of golden seal per dose.
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.
Formula KB packaged in 1 FL OZ (29mL) droppers. HoneyCombs Industries, 10671 6075 Road, Montrose, CO 81403.
Code information listed by FDA
375
Distribution and firm information
Recalling firm listed by FDA: HoneyCombs Industries, LLC
Firm location listed by FDA: Montrose, CO, United States
Distribution reported by FDA: Distributed nationwide to CO, MO, FL, NC, IN, MI, TN, KS, WI, OH, NM, AZ, GA, NY, TX, PA, MD, and KY. No foreign/VA/govt/military.
Product quantity listed by FDA: 133
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.