HoneyCombs Industries, LLC recalls Formula KB packaged in 1 FL OZ (29mL) droppers. HoneyCombs Industries, 10671 6075 Road, Montrose, CO 81403.
- Recall date
- August 4, 2015
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- F-3071-2015
- FDA classification
- Class II
- Brand / firm
- HoneyCombs Industries, LLC
- Sold / distributed
- 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.
Why it was recalled
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.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Formula KB packaged in 1 FL OZ (29mL) droppers. HoneyCombs Industries, 10671 6075 Road, Montrose, CO 81403.
Get recall alerts
Free email alert whenever HoneyCombs Industries, LLC has a new recall — straight from official government data. Unsubscribe anytime.
More recalls from: HoneyCombs Industries, LLC