AK Forte Ortiga y Omega 3 Cont. Neto 100 Tabletas recall
FDA recall D-0024-2025 · initiated Oct 8, 2024
C & A Naturistics recalled AK Forte Ortiga y Omega 3 Cont. Neto 100 Tabletas in Oct 2024 — an FDA Class II recall (D-0024-2025) because Marketed without an Approved NDA/ANDA: FDA analysis found the product to be tainted with undeclared diclofenac and acetaminophen.
May cause temporary or medically reversible harm; low probability of serious harm.
Why it was recalled
Marketed without an Approved NDA/ANDA: FDA analysis found the product to be tainted with undeclared diclofenac and acetaminophen.
Sold unapproved, or found to contain something undeclared
The product should not have been on sale in this form — often a supplement found to contain a hidden prescription drug.
This is a manufacturing or quality failure, not a finding that the medicine is unsafe to take — across every recall we hold, none was issued for that reason. It does not mean the batch was harmless.
Is your product affected? Check the lot number
A recall covers only specific lots. Find the lot number and expiration date on your package and compare them to the affected codes below — if yours is not listed, it was not part of this recall.
Quantity recalled: Unknown
Details
- Product
- AK Forte Ortiga y Omega 3 Cont. Neto 100 Tabletas, 400 mg,
- Recalling company
- C & A Naturistics
- Classification
- Class II
- Status
- Ongoing
- Type
- Voluntary: Firm initiated
- Distribution
- Nationwide within the United States
- Initiated
- Oct 8, 2024
- FDA report date
- Oct 30, 2024
Frequently asked
- Was AK Forte Ortiga y Omega 3 Cont. Neto 100 Tabletas recalled?
- C & A Naturistics recalled AK Forte Ortiga y Omega 3 Cont. Neto 100 Tabletas in Oct 2024 — an FDA Class II recall (D-0024-2025) because Marketed without an Approved NDA/ANDA: FDA analysis found the product to be tainted with undeclared diclofenac and acetaminophen. May cause temporary or medically reversible harm; low probability of serious harm.
- Why was AK Forte Ortiga y Omega 3 Cont. Neto 100 Tabletas recalled?
- Per the FDA enforcement record, the reason for recall D-0024-2025 was: Marketed without an Approved NDA/ANDA: FDA analysis found the product to be tainted with undeclared diclofenac and acetaminophen.
- Is a recalled AK Forte Ortiga y Omega 3 Cont. Neto 100 Tabletas dangerous to take?
- An FDA recall removes specific lots from the market for a defined reason and does not by itself mean the medicine is unsafe for everyone — your specific lot may never have been affected. May cause temporary or medically reversible harm; low probability of serious harm. Check the FDA notice for the affected lot numbers and expiration dates, and ask your pharmacist or doctor before stopping a prescribed medicine. This reproduces public FDA data and is not medical advice.
- Which lots of AK Forte Ortiga y Omega 3 Cont. Neto 100 Tabletas are affected?
- Distributed: Nationwide within the United States. The recall covers these lots — All Lots. Check the lot number and expiration date on your package against this list; if yours is not listed, it was not part of recall D-0024-2025.