Nutri-Dyn recalls 5-HTP Extra Strength supplements from Switzerland due to mislabeling during production. Affected products contain CoQ-10 but are labeled as 5-HTP. Consumers should check lot numbers and contact the company for details.
Nutri-Dyn has initiated a recall due to mislabeling. During production of CoQ-10, Lot #140186, one or more bottles were mistakenly labeled as 5-HTP Extra Strength.
Nutri-Dyn is recalling 5-HTP Extra Strength supplements that were mistakenly labeled as 5-HTP when they were actually CoQ-10. This mislabeling could lead to confusion about the supplement's contents and potential health effects.
The product was mislabeled during production, meaning bottles intended for CoQ-10 were incorrectly labeled as 5-HTP. This could cause consumers to take the wrong supplement, potentially leading to unintended health effects.
People who purchased the Nutri-Dyn 5-HTP Extra Strength supplements from Switzerland. Those with specific health conditions or taking other medications may be at higher risk due to potential interactions.
Check for the lot number 14086 on the product label. The product is a 60-capsule dietary supplement with UPC # 6 96859 02947 9 and SKU # R200E.
Look for the lot number 14086 on the product label to confirm if it's affected.
Nutri-Dyn initiated a recall due to mislabeling during production of CoQ-10, where some bottles were mistakenly labeled as 5-HTP Extra Strength.
Check the product label for lot number 14086. If it matches, contact Nutri-Dyn for further instructions.
The recall is for mislabeling, not a safety hazard. There is no risk of serious injury from this product.
We’ve drafted a message you can send Nutri-Dyn to request your refund or repair — edit it as you like.
Subject: Recall F-1922-2015 — Nutri-Dyn Nutri-Dyn Hello, I own a Nutri-Dyn that is covered by recall F-1922-2015 from Nutri-Dyn. 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.
