HoneyCombs Industries recalls Formula IM honey drops due to high coliform bacteria levels exceeding safety standards. Consumers should check product labels for the specific batch.
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 IM honey drops because they contain too much coliform bacteria. This could pose a health risk if consumed, especially for people with weakened immune systems.
The honey drops contain 2000 coliform bacteria per gram, which is above the safe limit of less than 1000 per gram. Coliform bacteria can cause foodborne illness, especially in vulnerable individuals.
Anyone who owns or uses Formula IM honey drops. People with compromised immune systems may be at higher risk due to potential bacterial contamination.
Check for Formula IM honey drops in 1 fl oz (29mL) dropper bottles. The product was manufactured by HoneyCombs Industries, LLC in Montrose, CO.
Look for the product name 'Formula IM' and the size '1 fl oz (29mL) dropper' on the bottle.
The recall indicates the product has higher coliform bacteria than safe levels, so it is not recommended for consumption.
Check for Formula IM honey drops in 1 fl oz (29mL) dropper bottles manufactured by HoneyCombs Industries, LLC in Montrose, CO.
The recall does not specify a remedy, so 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-3069-2015 — HoneyCombs HoneyCombs Hello, I own a HoneyCombs that is covered by recall F-3069-2015 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.
