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

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

Immuno - Dynamics is recalling Colostrum Lozenges, Dietary Supplement, Colostrum (Bovine) 200mg, 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 codesPerCoBa Lots: 627-20, 638-20. Synertek Lots: 627-20, 638-20.
Quantity recalledPerCoBa 3,310 units. Synertek 9,468 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-1015-2016
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 Lozenges, Dietary Supplement, Colostrum (Bovine) 200mg. Allergen statement: contains dairy. Packaged in the following sizes and Brand names: 1. PerCoBa, UPC 90576-00006. 100 Lozenges Distributed by: Immuno-Dynamics, Inc., Fennimore, WI 53809; 2. Synertek, UPC 90576-00007. 100 lozenges. 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

Is Colostrum Lozenges, Dietary Supplement, Colostrum (Bovine) 200mg recalled?

Yes. Immuno - Dynamics recalled Colostrum Lozenges, Dietary Supplement, Colostrum (Bovine) 200mg on 10 Nov 2015. The recall is Class III and its status is Terminated. Recall number F-1015-2016.

Why was it recalled?

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

Which lots are affected?

PerCoBa Lots: 627-20, 638-20. Synertek Lots: 627-20, 638-20.

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 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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