HoneyCombs Industries, LLC FDA recall records

The FDA has published 7 food recall enforcement records naming HoneyCombs Industries, LLC between 2015 and 2015, covering 1 separate recall events. The firm is recorded in Colorado. Data last updated 2 September 2026.

Records of 29,386
7
Share of all recalls
0%
Class I of 7
0
Reported between
2015 to 2015

What these records are

Every record on this page was published by the FDA in the openFDA food enforcement database. 7 records cover 1 recall events, because the agency opens one record per product code: a single recall of a product line with many codes appears here many times.

0 of these records are Class I, 7 Class II and 0 Class III. A recall count is not a safety score. Most FDA food recalls are initiated by the firm itself, and a recall is the firm removing product from the market, which is what a food safety plan is built to produce.

By year

Counts are by the date the FDA reported the enforcement action. That date runs behind the date a firm started a recall, so the most recent year is always partial.

Where the recalling firms are

The state is the location of the recalling firm, not where the product was sold. Distribution is recorded separately on each record.

Most recently reported

All 7 records.
ReportedProductFirmReasonClass
2015-09-09Expello-C packaged in 1 FL OZ (29mL) droppers. HoneyCombs Industries, 10671 6075 Road, Montrose, CO 81403.HoneyCombs Industries, LLCThe 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
2015-09-09Golden Seal Extract packaged in 1 FL OZ (29mL) droppers. HoneyCombs Industries, 10671 6075 Road, Montrose, CO 81403.HoneyCombs Industries, LLCThe 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
2015-09-09Formula L packaged in 1 FL OZ (29mL) droppers. HoneyCombs Industries, 10671 6075 Road, Montrose, CO 81403.HoneyCombs Industries, LLCThe 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
2015-09-09Formula KB packaged in 1 FL OZ (29mL) droppers. HoneyCombs Industries, 10671 6075 Road, Montrose, CO 81403.HoneyCombs Industries, LLCThe 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
2015-09-09Formula C&F packaged in 1 FL OZ (29mL) droppers. HoneyCombs Industries, 10671 6075 Road, Montrose, CO 81403.HoneyCombs Industries, LLCThe 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
2015-09-09Formula IM packaged in 1 FL OZ (29mL) droppers. HoneyCombs Industries, 10671 6075 Road, Montrose, CO 81403.HoneyCombs Industries, LLCThe 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
2015-09-09Formula E packaged in 1 FL OZ (29mL) droppers. HoneyCombs Industries, 10671 6075 Road, Montrose, CO 81403.HoneyCombs Industries, LLCThe 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

Questions

How many FDA recalls has HoneyCombs Industries, LLC had?
The FDA has published 7 food recall enforcement records naming HoneyCombs Industries, LLC between 2015 and 2015. Those records cover 1 separate recall events: the agency opens one record per product code, so one recall of a product line appears as many records.
Does a high recall count mean a firm is unsafe?
Not on its own. Most FDA food recalls are initiated voluntarily by the firm, and a recall is the firm removing product from the market, which is what a working food safety plan is supposed to produce. Record counts also scale with the number of product codes a firm carries rather than with the number of things that went wrong.

All FDA food recall data

A recall is the end of an evidence trail that either existed or did not. Krolda maps supplier documents to the clause they satisfy in FSSC 22000, IFS Food and 21 CFR 117, and routes the corrective action when the evidence is missing.

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