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Class II: temporary or reversible health riskTerminated

HoneyCombs Industries Formula L packaged in 1 FL OZ Recall

Formula L packaged in 1 FL OZ (29mL) droppers

HoneyCombs Industries, LLC · Montrose, CO

Risk level
Class II
Reported by FDA
Sep 9, 2015
Recall ID
F-3072-2015
Check your lot numberHow we source this data

Summary

HoneyCombs Industries recalled Formula L packaged in 1 FL OZ starting Aug 4, 2015. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report F-3072-2015 on Sep 9, 2015. Reason: 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. Status: Terminated.

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.

Product description

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

Lot numbers, UPCs & expiration codes

380

Where it was 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 to do if you have this product

  • Compare the brand, size, and lot/UPC codes on your package with the codes above.
  • If it matches, don't eat it. Return it to the store for a refund or throw it away.
  • Wash surfaces and containers that touched the product.
  • If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall details

Recall number
F-3072-2015
Classification
Class II
Status
Terminated
Recall initiated
Aug 4, 2015
FDA report date
Sep 9, 2015
Quantity
68
Recall type
Voluntary: Firm initiated
Recalling firm
HoneyCombs Industries, LLC

Original FDA data

Every field from FDA enforcement report F-3072-2015, exactly as published.

Show all FDA fields
City
Montrose
State
CO
Status
Terminated
Country
United States
Event ID
71890
Address
10671 6075 Rd
Code information
380
Postal code
81403-8957
Report date
Sep 9, 2015
Product type
Food
Recall number
F-3072-2015
Classification
Class II
Recalling firm
HoneyCombs Industries, LLC
Product quantity
68
Termination date
Mar 2, 2017
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.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Formula L packaged in 1 FL OZ (29mL) droppers. HoneyCombs Industries, 10671 6075 Road, Montrose, CO 81403.
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.
Recall initiation date
Aug 4, 2015
Initial firm notification
Letter
Center classification date
Aug 28, 2015

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-3072-2015, published Sep 9, 2015. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

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