Class IITerminated in FDA datasetAug 4, 2015

Formula E packaged in 1 FL OZ (29mL) droppers. HoneyCombs Industries, 10671 6075 Road, Montrose, CO 81403.

Recalling firm: HoneyCombs Industries, LLC

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.

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ProductFormula E packaged in 1 FL OZ (29mL) droppers. HoneyCombs Industries, 10671 6075 Road, Montrose, CO 81403.

FDA code information

350

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Full FDA record and distribution details

Original product description

Formula E packaged in 1 FL OZ (29mL) droppers. HoneyCombs Industries, 10671 6075 Road, Montrose, CO 81403.

Recall details

Recall number
F-3070-2015
Event ID
71890
FDA status
Terminated
Initiated
Aug 4, 2015
Reported
Sep 9, 2015
Classified
Aug 28, 2015
Terminated
Mar 2, 2017
Quantity
72
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.

FDA source record · F-3070-2015

Data updated September 16, 2026. View official FDA data ↗

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