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RECALL RECORD — CLASS IIIRecall closedF-1015-2016/FDA enforcement
Immuno - Dynamics, INC·Dietary Supplements·Nov 10, 2015

Colostrum Lozenges, Dietary Supplement, Colostrum (Bovine) 200mg

What you need to know

Class III

  • What happened

    The PerCoBa brand and Synertek brand Colostrum product labels should state contains milk.

  • Health risk

    The product is unlikely to cause adverse health consequences. These recalls are often related to labeling or quality violations. A safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

  • 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 FDANationwide (US)More supplements

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Product identification

Source: FDA FOOD

Brand nameImmuno - Dynamics, INC
Recalling firmImmuno - Dynamics, INCFennimore, WI, United States
UPC / barcodesNo UPC listed in the FDA enforcement record.
Lot / date codes
  • PerCoBa Lots: 627-20, 638-20. Synertek Lots: 627-20, 638-20.
Distribution area
Nationwide

Nationwide to include Puerto Rico. Outside the US to include: Australia, Canada, Finland, France, Germany, Greece, Ireland, Israel, Italy, Malaysia, Mexico, Netherlands, Norway, Russian Federation, Singapore, Sri Lanka, Sweden, Thailand, Turkey, United Kingdom (Great Britain).

United States, Canada, Mexico, United Kingdom, Australia, Germany, France, Puerto Rico

Quantity affectedPerCoBa 3, 310 units. Synertek 9, 468 units.
Recall initiationFDA report date: April 13, 2016
FDA recall numberF-1015-2016

Beyond the headline

The recall, in context

Immuno - Dynamics, INC initiated this supplements recall on November 10, 2015. The FDA enforcement report states: The PerCoBa brand and Synertek brand Colostrum product labels should state contains milk. The FDA report lists distribution as: Nationwide to include Puerto Rico. Outside the US to include: Australia, Canada, Finland, France, Germany, Greece, Ireland, Israel, Italy, Malaysia, Mexico, Netherlands, Norway, Russian Federation, Singapore, Sri Lanka, Sweden, Thailand, Turkey , United Kingdom (Great Britain).

The FDA enforcement report describes the reason as: The PerCoBa brand and Synertek brand Colostrum product labels should state contains milk.

Colostrum Lozenges, Dietary Supplement, Colostrum (Bovine) 200mg was made or distributed by Immuno - Dynamics, INC in Fennimore, WI, United States. This page reflects FDA report F-1015-2016, dated April 13, 2016.

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, a safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

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 lot and date codes 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 milk

Symptoms to watch for

Hives, swelling, wheezing, vomiting or anaphylaxis can occur in people with a milk allergy.

When symptoms may appear

Reactions can begin within minutes to a few hours after eating the product.

Higher-risk groups

People with a diagnosed cow's milk allergy, especially children and anyone with a history of anaphylaxis.

What to do now

  1. 1Do not eat the product if you have a milk allergy.
  2. 2Seek emergency care for breathing difficulty, throat swelling or other signs of anaphylaxis.
  3. 3Keep the packaging and contact the retailer or manufacturer about a refund.

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 Colostrum Lozenges, Dietary Supplement, Colostrum (Bovine) 200mg recall?

Immuno - Dynamics, INC recalled Colostrum Lozenges, Dietary Supplement, Colostrum (Bovine) 200mg in an FDA Class III enforcement action reported as F-1015-2016. The PerCoBa brand and Synertek brand Colostrum product labels should state contains milk.

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 the product if you have a milk allergy. Seek emergency care for breathing difficulty, throat swelling or other signs of anaphylaxis. Keep the packaging and contact the retailer or manufacturer about a refund.

Is the Immuno - Dynamics, 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-1015-2016. 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

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