AK Forte: AK Forte Dietary Supplement — FDA announcement Oct 16, 2024

Published notice; closure not supplied

A company announcement posted by FDA. The listing date can differ from the original announcement date. The absence of a termination marker does not prove the recall is currently ongoing.

Source date Oct 16, 2024. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.

What the record says

Product
AK Forte Dietary Supplement
Reason
Device & Drug Safety – Unapproved Drug
Classification
Not supplied
Recalling firm
C&A Naturistics
Quantity
Not supplied
Agency-reported status
Company recall announcement
Source record identifier
9da4ab816f3fc6c6

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Lot and product identifiers

Label fieldDetails supplied by the agency
Lot, code or applicabilityNot supplied

Match all identifying details in the current notice. A brand name alone is not enough.

Distribution

AK Forte is marketed as a dietary supplement for Joint pain and Arthritis and is packaged in a cardbox type of packaging, with white, blue, red and gold logo of AK with a gold crown on top with 100 tablets per units, and all codes. The affected product AK Forte, all lots were distributed Nationwide via our Ebay and Etsy store.

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

Dates in the source

Fda listing date
Oct 16, 2024
Company announcement date
Oct 8, 2024

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

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