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RECALL RECORD — CLASS IIIRecall closedF-1922-2015/FDA enforcement
Nutri-dyn Midwest, INC.·Dietary Supplements·Nov 17, 2014

Nutri-dyn, 5-htp Extra Strength, Pharmaceutical Grade from Switzerland, Dietary Supplement 60…

What you need to know

Class III

  • What happened

    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.

  • Health risk

    The product is unlikely to cause adverse health consequences. These recalls are often related to labeling or quality violations. An allergen that is present but missing or incorrect on the label can cause a serious reaction in allergic consumers.

  • Action required

    Stop taking the supplement. Check the lot and UPC codes below, then return it to the retailer or contact the manufacturer about a refund. Seek medical advice if you have concerns about exposure.

Recall closed · classified by the FDAAZ, CO, IA, IN +9 moreMore supplements

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Match before you discard

Product identification

Source: FDA FOOD

Brand nameNutri-dyn Midwest, INC.
Recalling firmNutri-dyn Midwest, INC.Maple Plain, MN, United States
UPC / barcodes
6 96859 02947 9
Lot / date codes
  • Lot # 14086
Distribution area
AZCOIAINMIMNMTMDNJNYSDTXWI

US: AZ, CO, IA, IN, MI, MN, MT, MD, NJ, NY, SD, TX, WI. OUS: ISRAEL

United States

Quantity affected1, 627 bottles
Recall initiationFDA report date: April 15, 2015
FDA recall numberF-1922-2015

Beyond the headline

The recall, in context

Nutri-dyn Midwest, INC. initiated this supplements recall on November 17, 2014. The FDA enforcement report states: 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. The FDA report lists distribution as: US: AZ, CO, IA, IN, MI, MN, MT, MD, NJ, NY, SD, TX, WI. OUS: ISRAEL.

The FDA enforcement report describes the reason as: 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, 5-htp Extra Strength, Pharmaceutical Grade from Switzerland, Dietary Supplement 60… was made or distributed by Nutri-dyn Midwest, INC. in Maple Plain, MN, United States. This page reflects FDA report F-1922-2015, dated April 15, 2015.

Why this is a Class III recall

Class III means the product is unlikely to cause adverse health consequences. These recalls are often related to labeling or quality violations. In this recall, an allergen that is present but missing or incorrect on the label can cause a serious reaction in allergic consumers.

FDA definition

The product is unlikely to cause adverse health consequences. These recalls are often related to labeling or quality violations.

What to do now

  1. 1

    Stop using it

    Do not eat, drink or take the affected product.

  2. 2

    Check the codes

    Compare the UPC and lot code against the table above.

  3. 3

    Return or discard

    Contact the retailer or recalling firm about a refund, and dispose of the product safely.

Consumer safety guide

Undeclared allergen

Symptoms to watch for

Hives, swelling, wheezing, coughing, vomiting, abdominal pain or a drop in blood pressure. Anaphylaxis is a medical emergency.

When symptoms may appear

Allergic reactions often begin within minutes to a few hours of eating the allergen.

Higher-risk groups

Anyone with a diagnosed food allergy, especially children, and people with a history of anaphylaxis or asthma.

What to do now

  1. 1Do not eat or serve the affected product if you or anyone in the household has a diagnosed allergy.
  2. 2If symptoms such as swelling, wheezing or breathing difficulty occur, use the person's prescribed emergency plan and call emergency services.
  3. 3Keep the packaging, contact the retailer or manufacturer for a refund, and read the official recall notice for the exact allergen.

For a severe allergic reaction, do not wait for a callback or refund process before seeking emergency care.

This is general consumer safety information, not medical advice or a diagnosis. Follow the official recall notice and contact a healthcare professional if you have concerns about exposure or symptoms.

Frequently asked

Questions about this recall

What is the Nutri-dyn, 5-htp Extra Strength, Pharmaceutical Grade from Switzerland, Dietary Supplement 60… recall?

Nutri-dyn Midwest, INC. recalled Nutri-dyn, 5-htp Extra Strength, Pharmaceutical Grade from Switzerland, Dietary Supplement 60… in an FDA Class III enforcement action reported as F-1922-2015. 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.

What should I do if I bought this product?

Stop taking the supplement. Check the lot and UPC codes below, then return it to the retailer or contact the manufacturer about a refund. Seek medical advice if you have concerns about exposure. Do not eat or serve the affected product if you or anyone in the household has a diagnosed allergy. If symptoms such as swelling, wheezing or breathing difficulty occur, use the person's prescribed emergency plan and call emergency services. Keep the packaging, contact the retailer or manufacturer for a refund, and read the official recall notice for the exact allergen.

Is the Nutri-dyn Midwest, INC. recall still active?

The FDA lists this recall as recall closed. It remains relevant if you still have the affected product or need to identify a historical recall.

Where can I verify this recall?

This page is normalized from the openFDA enforcement record F-1922-2015. You can verify it directly using the official source link on this page. VerifyRecall updates its index from public FDA enforcement data and does not replace advice from the FDA, the recalling firm or a healthcare professional.

Verify before you act.

VerifyRecall is independent and not affiliated with the FDA. Always confirm the latest status on the official source record.

Official source

Brand history

More recalls by Nutri-dyn Midwest, INC.

View brand
Class II·

Nutri-dyn Midwest, INC.

Nutri-dyn Calcium D-glucarate Plus, Dietary Supplement, 60 Capsules

During production of St. John's Wort, Lot 160876, a number of bottles were mistakenly labeled as Calcium D-Glucarate Plus

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Record last synced from official openFDA enforcement data on November 14, 2026. Source record: official FDA notice.