Recall record at a glance
| Official record | F-3069-2015 |
|---|---|
| Category | Food Recalls |
| Classification | Class II |
| FDA record status | Terminated |
| Recalling firm | HoneyCombs Industries, LLC |
| Report date | Sep 9, 2015 |
| Recall initiation date | Aug 4, 2015 |
| Quantity | 55 botltes |
| Location | Montrose, CO, United States |
Official product description
Formula IM packaged in 1 FL OZ (29mL) droppers. HoneyCombs Industries, 10671 6075 Road, Montrose, CO 81403.
Why the product was recalled
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.
Distribution information
Distributed nationwide to CO, MO, FL, NC, IN, MI, TN, KS, WI, OH, NM, AZ, GA, NY, TX, PA, MD, and KY. No foreign/VA/govt/military.
How to read the classification
FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.
Additional record details
Recall type: Voluntary: Firm initiated. Initial notification: Letter.
What to do next
If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.
About this record
Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.
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