HoneyCombs Industries recalls Formula KB honey drops due to high coliform bacteria levels. The product may pose health risks if consumed. Consumers should check for the specific packaging and contact HoneyCombs for details.
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.
HoneyCombs Industries is recalling Formula KB honey drops because they contain a high level of coliform bacteria (2000 cfu/g) instead of the required less than 1000 cfu/g. This could lead to health issues if consumed.
The honey drops contain a coliform count of 2000 cfu/g, which is above the required limit of less than 1000 cfu/g. Coliform bacteria can cause foodborne illnesses, especially in vulnerable populations like infants.
Anyone who owns or uses Formula KB honey drops packaged in 1 fl oz droppers. Children and infants are at higher risk due to their smaller body size and potential for higher exposure.
Check for Formula KB honey drops in 1 fl oz (29mL) droppers with the HoneyCombs Industries label. The product was sold by HoneyCombs Industries in Montrose, CO.
Look for the product name 'Formula KB' and the packaging size of 1 fl oz (29mL) droppers.
The recall indicates a high coliform count, which could pose health risks. Consumers should not use the product until further instructions are received.
The recall record does not specify any remedy or replacement options.
The recall does not mention any risk of serious injury; the hazard is related to potential foodborne illness.
We’ve drafted a message you can send HoneyCombs to request your refund or repair — edit it as you like.
Subject: Recall F-3071-2015 — HoneyCombs HoneyCombs Hello, I own a HoneyCombs that is covered by recall F-3071-2015 from HoneyCombs. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
