HoneyCombs Industries recalls Formula E honey droppers due to high coliform bacteria levels exceeding safety standards. Consumers should check product labels for 1 FL OZ droppers.
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 E honey in 1 fl oz droppers because the powdered golden seal has a coliform count of 2000 cfu/g, which is higher than the required less than 1000 cfu/g. This could pose a risk of foodborne illness if consumed.
The honey contains a coliform count of 2000 cfu/g, which exceeds the safety standard of less than 1000 cfu/g. Coliform bacteria can cause foodborne illnesses, but the risk is low as the product is not intended for direct consumption in large quantities.
Anyone who purchased Formula E honey in 1 fl oz droppers from HoneyCombs Industries. Children and elderly individuals may be at slightly higher risk due to potential foodborne illness.
Check for Formula E honey in 1 fl oz (29mL) droppers with the manufacturer address: 10671 6075 Road, Montrose, CO 81403. The product was sold in quantities of 350.
Look for the product name 'Formula E' and the size '1 fl oz (29mL) droppers' on the label.
The recall is due to high coliform bacteria levels, but the product is not considered immediately dangerous. Consumers should check the recall details before use.
The record states 350 units were sold, but the exact number of affected items is not specified.
The recall record does not specify a remedy, so consumers should check the product label and contact HoneyCombs Industries for further instructions.
We’ve drafted a message you can send HoneyCombs to request your refund or repair — edit it as you like.
Subject: Recall F-3070-2015 — HoneyCombs HoneyCombs Hello, I own a HoneyCombs that is covered by recall F-3070-2015 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.
