Formula C&F packaged in 1 FL OZ — Class II food recall F-3068-2015
Terminated recall by HoneyCombs Industries, LLC, reported 2015-09-09, distributed nationwide. The powdered golden seal had a coliform count of 2000 cfu/g when the specifications stated less than 1000/cfy/
| Recall number | F-3068-2015 |
|---|---|
| Product type | Food |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | HoneyCombs Industries, LLC, Montrose, CO, United States |
| Recall initiated | 2015-08-04 |
| Classified | 2015-08-28 |
| Reported by FDA | 2015-09-09 |
| Terminated | 2017-03-02 |
| Distributed | Nationwide (US) |
| Quantity | 161 bottles |
| Reason classes | packaging |
Product
Formula C&F 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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/F-3068-2015. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.