HoneyCombs Industries recalls Formula C&F 1 fl oz droppers due to high coliform bacteria levels in golden seal powder, which may pose health risks.
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 C&F packaged in 1 fl oz droppers because the golden seal powder contains 2000 coliform bacteria per gram, exceeding the safety limit of less than 1000 per gram. This could lead to potential health issues from consuming contaminated products.
The golden seal powder in the product contains 2000 coliform bacteria per gram, which is above the safety standard of less than 1000 per gram. Coliform bacteria can indicate contamination and may cause gastrointestinal issues if consumed in large amounts.
People who purchased Formula C&F 1 fl oz droppers from HoneyCombs Industries in the U.S. are affected. Those with sensitive digestive systems or compromised immune systems may be at slightly higher risk.
Check for Formula C&F packaged in 1 fl oz (29mL) droppers from HoneyCombs Industries. The product was sold in the U.S. and has a lot number of 330.
Look for the product name and lot number on the packaging to confirm if it matches the recalled items.
The recall indicates the product may have higher coliform bacteria than safe levels, but the official notice does not specify if it is safe to use.
Check for Formula C&F packaged in 1 fl oz (29mL) droppers with lot number 330 from HoneyCombs Industries.
The recall notice does not provide specific action steps for consumers, so you should check with 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-3068-2015 — HoneyCombs HoneyCombs Hello, I own a HoneyCombs that is covered by recall F-3068-2015 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.
