CLASS II Food recall · Reported 9 Sep 2015 · FDA Enforcement Report

Formula E recalled by HoneyCombs Industries

HoneyCombs Industries is recalling Formula E, distributed nationwide in the US. The recall was initiated on 4 Aug 2015 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codes350
Quantity recalled72

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-3070-2015
FDA event ID
71890
Recalling firm
HoneyCombs Industries, Montrose, CO
Classification
Class II
Status
Terminated
Recall initiated
4 Aug 2015
FDA classified
28 Aug 2015
Reported
9 Sep 2015
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Packaging Defects
Product category
Honey & Syrup

Timeline

4 Aug 2015Recall initiated by company
28 Aug 2015Classified by FDA+24 days
9 Sep 2015Published in enforcement report+12 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

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.

Packaging recalls include wrong labels, wrong products in the wrong bottle, missing leaflets, short-filled or empty capsules and seals that fail.

Product as listed by the FDA

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

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.

Nationwide ArizonaColoradoFloridaGeorgiaIndianaKansasKentuckyMarylandMichiganMissouriNorth CarolinaNew MexicoNew YorkOhioPennsylvaniaTennesseeTexasVirginiaWisconsin

Questions about this recall

Is Formula E recalled?

Yes. HoneyCombs Industries recalled Formula E on 4 Aug 2015. The recall is Class II and its status is Terminated. Recall number F-3070-2015.

Why was it 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.

Which lots are affected?

350

Where was it sold?

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.

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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