FDA (Food) recall action 71890
The FDA (Food) publishes a recall like this one as 7 separate product records. They share a firm, a date and a cause; this page is all of them in one place, so the scale of the action is visible rather than spread across 7 pages.
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.
The agency’s own wording, quoted from the enforcement report.
The unit total adds up the quantities the agency stated for each product. Where a product record gave no figure, or gave a weight rather than a count, it contributes nothing — so the real total is at least this, never less.
HoneyCombs Industries is recalling Formula E droppers due to coliform counts exceeding specifications. The product was distributed nationwide.
HoneyCombs Industries is recalling 133 units of Formula KB droppers because the powdered golden seal ingredient contained coliform bacteria levels above the specified limit.
HoneyCombs Industries is recalling 161 bottles of Formula C&F droppers because the powdered golden seal ingredient contained coliform bacteria levels exceeding specifications.
HoneyCombs Industries is recalling 262 bottles of Expello-C because the powdered golden seal ingredient contained coliform bacteria levels exceeding specifications.
HoneyCombs Industries is recalling 68 units of Formula L droppers due to coliform counts exceeding specifications.
HoneyCombs Industries is recalling 432 bottles of Golden Seal Extract because the product contained higher levels of coliform bacteria than allowed by specifications.
HoneyCombs Industries is recalling 55 bottles of Formula IM because the powdered golden seal ingredient contained coliform bacteria levels above the specified limit.