F-3070-2015 Class II Terminated
FDA food recall F-3070-2015 was initiated by HoneyCombs Industries, LLC on August 4, 2015 and is designated Class II. Reason for recall: 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. The recall status is terminated (terminated March 2, 2017). Affected quantity: 72.
Recall Details
- Product Type
- Food
- Report Date
- September 9, 2015
- Initiation Date
- August 4, 2015
- Termination Date
- March 2, 2017
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 72
Product Description
Formula E packaged in 1 FL OZ (29mL) droppers. HoneyCombs Industries, 10671 6075 Road, Montrose, CO 81403.
Reason for Recall
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.
Distribution Pattern
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.
Code Information
350