HoneyCombs Formula L Recalled for Excessive Coliform Bacteria
HoneyCombs Industries is recalling 68 units of Formula L droppers due to coliform counts exceeding specifications.
The agency’s classification
FDA (Food): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 2/5 (Moderate).
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: The recall is classified as FDA Class II, but the source text does not report any illnesses or injuries, fitting the criteria for a moderate severity recall involving low-risk contamination or voluntary precautionary measures.
Plain-English summary
HoneyCombs Industries, LLC is recalling 68 units of Formula L, a powdered golden seal supplement packaged in 1 FL OZ (29mL) droppers. The recall was initiated because the product had a coliform count of 2000 cfu/g, which exceeded the specified limit of less than 1000 cfu/g. Each dose contains 12mg of golden seal.
The affected product was distributed nationwide to Colorado, Missouri, Florida, North Carolina, Indiana, Michigan, Tennessee, Kansas, Wisconsin, Ohio, New Mexico, Arizona, Georgia, New York, Texas, Pennsylvania, Maryland, and Kentucky. The recall does not include foreign, VA, government, or military distribution channels.
Consumers who purchased this product should stop using it and contact the manufacturer for further instructions.
The recalled product
- Product
- Formula L packaged in 1 FL OZ (29mL) droppers. HoneyCombs Industries, 10671 6075 Road, Montrose, CO 81403.
- Manufacturer
- HoneyCombs Industries, LLC
- Category
- Food — Dietary Supplement
- Hazard
- Affected units
- 68
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- 380
Distribution
Part of a larger recall action
This product is one of 7 recalled by HoneyCombs Industries, LLC under a single FDA (Food) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
See all 7 products in this recall →Related recalls
Same manufacturer · HoneyCombs Industries, LLC
See all →- ModerateHoneyCombs Industries Recalls Expello-C Due to High Coliform Counts
FDA (Food) · 2015-09-09
- ModerateHoneyCombs Recalls Golden Seal Extract Due to High Coliform Count
FDA (Food) · 2015-09-09
- ModerateHoneyCombs Formula KB Recalled for Excessive Coliform Bacteria
FDA (Food) · 2015-09-09
- ModerateHoneyCombs Formula C&F Recalled for Excessive Coliform Bacteria
FDA (Food) · 2015-09-09
- ModerateHoneyCombs Formula E Recalled for Excessive Coliform Bacteria
FDA (Food) · 2015-09-09
Same hazard · bacterial contamination
See all →- HighClorox Recalls Scented Mistolin and Lestoil Cleaners in Puerto Rico
CPSC · 2026-09-03
- HighCurry chicken salad flagged for possible Listeria contamination in two states
USDA FSIS · 2026-07-30
- ModerateMedline Medical Convenience Kits Recalled Due to Potential Bacillus Contamination
FDA (Devices) · 2026-07-29
- HighMedline Convenience Kits Recalled Over Bacillus Contamination
FDA (Devices) · 2026-07-29
- SevereSurgical Convenience Kit Recalled for Bacterial Contaminant in Alcohol Prep Pads
FDA (Devices) · 2026-07-08
Similar recalls
- LowHetero USA Recalls Montelukast Sodium Tablets Due to Discoloration
FDA (Drugs) · 2017-04-05
- HighVitaminAlly FulviLife Complex recalled over manufacturing practice deviations
FDA (Food) · 2026-05-27
- ModerateBeaumont Bio-Med Recalls Diarrhea Response Homeopathic Formula Due to CGMP Deviations
FDA (Drugs) · 2018-09-26
- HighLiquid supplement shots recalled over possible coliforms and E. coli
FDA (Food) · 2026-02-18
- HighVitaminAlly womens 50+ multivitamin drops recalled over manufacturing deviations
FDA (Food) · 2026-05-27
- SevereRed Diamond Coffee Concentrate Recalled for Elevated pH Levels
FDA (Food) · 2016-02-24