Formula C&F packaged in 1 FL OZ (29mL) droppers. HoneyCombs Industries, 10671 6075 Road,…
Recalling firm: HoneyCombs Industries, LLC
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.
Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Mar 2, 2017.
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FDA code information
330
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Full FDA record and distribution details
Original product description
Formula C&F packaged in 1 FL OZ (29mL) droppers. HoneyCombs Industries, 10671 6075 Road, Montrose, CO 81403.
Original FDA recall 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.
Recall details
- Recall number
- F-3068-2015
- Event ID
- 71890
- FDA status
- Terminated
- Initiated
- Aug 4, 2015
- Reported
- Sep 9, 2015
- Classified
- Aug 28, 2015
- Terminated
- Mar 2, 2017
- Quantity
- 161 bottles
- Location
- Montrose, CO, United States
- Initiation type
- Voluntary: Firm initiated
- Notification
- Letter
Where it was 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.
Data updated September 16, 2026. View official FDA data ↗
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