CLASS III Food recall · Reported 13 Apr 2016 · FDA Enforcement Report

Colostrum Powder, Dietary Supplement, Allergen statement recalled

Immuno - Dynamics is recalling Colostrum Powder, Dietary Supplement, Allergen statement: contains dairy, distributed nationwide in the US. The recall was initiated on 10 Nov 2015 and the FDA has classified it as Class III.

Check your package

Lot, batch or date codes250 gram jar Lots: 627-30, 628-30, 628-31, 630-31, 632-30, 633-30, 633-31, 635-30, 635-35, 636-30, 637-30, 637-31, 638-30, 638-31, 639-30, 639-31, 639-32, 641-30, 642-30, 644-30, 644-31, 646-30. 150 gram Jar Lots: 642-100 8.8 ounce jar Lots: 627-30, 628-30, 628-31, 630-31, 632-30, 633-30, 633-31, 635-30, 635-35, 636-30, 637-30, 637-31, 638-30, 638-31, 639-30, 639-31, 639-32, 641-30, 642-30, 644-30, 644-31, 646-30
Quantity recalled250 gram jars - 2,532 units. 150 gram jars - 68 units. 8.8 ounce jars - 11,008 units

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-1013-2016
FDA event ID
72665
Recalling firm
Immuno - Dynamics, Fennimore, WI
Classification
Class III
Status
Terminated
Recall initiated
10 Nov 2015
FDA classified
4 Apr 2016
Reported
13 Apr 2016
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Undeclared Allergens
Product category
Dietary Supplements

Timeline

10 Nov 2015Recall initiated by company
4 Apr 2016Classified by FDA+146 days
13 Apr 2016Published in enforcement report+9 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

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

Food allergen labelling is required by US law for the nine major allergens. A product recalled for an undeclared allergen is only a risk to people with that allergy; everyone else can consume it safely.

Product as listed by the FDA

Colostrum Powder, Dietary Supplement, Allergen statement: contains dairy. Colostrum (bovine) packaged in the following sizes and brand names: 1. PerCoBa Extra Edge Net Weight 150 grams, UPC 90576-00099. 3,000 mg Colostrum (bovine) per 2 teaspoons. Immuno-Dynamics, Inc., 1800 Dodge Street, Fennimore, WI 53809; 2. PerCoBa Extra Edge Net Weight 250 grams, UPC 90576-00001. 3,000 mg Colostrum (bovine) per 2 teaspoons. Immuno-Dynamics, Inc., 1800 Dodge Street, Fennimore, WI 53809.; 3. Synertek Balanced Pure, 8.8 ounces, UPC 09408-29292. 1,500 mg Colostrum (bovine) per 1 teaspoon. Distributed by Synertek Colostrum, Inc., Cheyenne, WY 82009.

Where it was distributed

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).

Nationwide Puerto Rico

Questions about this recall

Why was it recalled?

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

Which lots are affected?

250 gram jar Lots: 627-30, 628-30, 628-31, 630-31, 632-30, 633-30, 633-31, 635-30, 635-35, 636-30, 637-30, 637-31, 638-30, 638-31, 639-30, 639-31, 639-32, 641-30, 642-30, 644-30, 644-31, 646-30. 150 gram Jar Lots: 642-100 8.8 ounce jar Lots: 627-30, 628-30, 628-31, 630-31, 632-30, 633-30, 633-31, 635-30, 635-35, 636-30, 637-30, 637-31, 638-30, 638-31, 639-30, 639-31, 639-32, 641-30, 642-30, 644-30, 644-31, 646-30

Where was it sold?

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).

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class III mean?

Class III recalls are for products unlikely to cause any adverse health consequence, usually labelling or quality issues.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

4 other products · FDA event 72665

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