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

PerCoBa 1, Colostral Whey, Dietary Supplement recalled

Immuno - Dynamics is recalling PerCoBa 1, Colostral Whey, Dietary Supplement, Colostral Whey Protein 4%. Net Contents, distributed nationwide in the US. The recall was initiated on 10 Nov 2015 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLots: 477, 479, 481, 484.
Quantity recalled2,815 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-1016-2016
FDA event ID
72665
Recalling firm
Immuno - Dynamics, Fennimore, WI
Brand
PerCoBa
Classification
Class II
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
Other Reasons
Product category
Protein Powder

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.

Product as listed by the FDA

PerCoBa 1, Colostral Whey, Dietary Supplement, Colostral Whey Protein 6.4%. Net Contents: 4 oz. Immuno-Dynamics, Inc. , PO Box 544 Perry, Iowa 50220

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

Is PerCoBa 1, Colostral Whey, Dietary Supplement, Colostral Whey Protein 4%. Net Contents recalled?

Yes. Immuno - Dynamics recalled PerCoBa 1, Colostral Whey, Dietary Supplement, Colostral Whey Protein 4%. Net Contents on 10 Nov 2015. The recall is Class II and its status is Terminated. Recall number F-1016-2016.

Why was it recalled?

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

Which lots are affected?

Lots: 477, 479, 481, 484.

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 II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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