HoneyCombs Industries recalls Formula L honey in 1 fl oz droppers due to high coliform count in powdered golden seal. This may pose a food safety risk.
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 L honey in 1 fl oz droppers because the powdered golden seal has a coliform count of 2000 cfu/g, which exceeds the required standard of less than 1000 cfu/g. This could pose a food safety risk if consumed.
The powdered golden seal in Formula L honey has a coliform count of 2000 cfu/g, which is higher than the required standard of less than 1000 cfu/g. Coliform bacteria can indicate contamination and potentially cause foodborne illness.
Owners of Formula L honey in 1 fl oz droppers from HoneyCombs Industries in Montrose, CO are affected. Those with the product may be at risk if they consume it.
Check for Formula L honey 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 L' and the size '1 fl oz (29mL) droppers' on the label.
The powdered golden seal in Formula L honey has a coliform count of 2000 cfu/g, which exceeds the required standard of less than 1000 cfu/g.
The recall notice does not specify a remedy.
The high coliform count may indicate contamination and could pose a food safety risk, but the recall does not specify serious injury risks.
We’ve drafted a message you can send HoneyCombs to request your refund or repair — edit it as you like.
Subject: Recall F-3072-2015 — HoneyCombs HoneyCombs Hello, I own a HoneyCombs that is covered by recall F-3072-2015 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.