FDA found C & A Naturistics AK Forte Ortiga y Omega 3 Cont. Neto 100 Tabletas contain undeclared diclofenac and acetaminophen. All lots recalled due to unapproved medication content.
Marketed without an Approved NDA/ANDA: FDA analysis found the product to be tainted with undeclared diclofenac and acetaminophen.
C & A Naturistics recalled all lots of AK Forte Ortiga y Omega 3 Cont. Neto 100 Tabletas (400 mg) because the FDA found they contain undeclared diclofenac and acetaminophen. This poses a risk of medication interactions or adverse effects since these drugs were not approved for this product.
The product was marketed without FDA approval and contains undeclared diclofenac (a painkiller) and acetaminophen (a common pain reliever). These medications were not intended to be in this supplement and could cause harmful interactions or side effects if taken without proper medical supervision.
People who purchased or use this dietary supplement product are affected. Those with existing conditions requiring specific medications may be at higher risk due to potential interactions.
Check for the product name 'AK Forte Ortiga y Omega 3 Cont. Neto 100 Tabletas, 400 mg' on the label. All lots of this product are affected and have been recalled.
Immediately stop using the recalled product as it contains undeclared medications that could cause harm.
No, the FDA found this product contains undeclared diclofenac and acetaminophen, which were not approved for this product and could cause harm.
Check the label for 'AK Forte Ortiga y Omega 3 Cont. Neto 100 Tabletas, 400 mg' — all lots are affected.
Immediately stop using it and contact the manufacturer for instructions on disposal or return.
We’ve drafted a message you can send C & A Naturistics to request your refund or repair — edit it as you like.
Subject: Recall D-0024-2025 — C & A Naturistics C & A Naturistics Hello, I own a C & A Naturistics that is covered by recall D-0024-2025 from C & A Naturistics. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
