Class IIITerminated in FDA datasetNov 10, 2015

Colostrum Lozenges, Dietary Supplement, Colostrum (Bovine) 200mg. Allergen statement: contains dairy. Packaged in the following sizes and Brand names: 1. PerCoBa

Recalling firm: Immuno - Dynamics, Inc

Why it was recalled

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

Check your package

Compare the exact product and package details with the label you have.

ProductColostrum 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.

FDA code information

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

Match the product, package size, and code together. A missing match does not guarantee safety.

Full FDA record and distribution details

Original product description

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.

Recall details

Recall number
F-1015-2016
Event ID
72665
FDA status
Terminated
Initiated
Nov 10, 2015
Reported
Apr 13, 2016
Classified
Apr 4, 2016
Terminated
May 10, 2016
Quantity
PerCoBa 3,310 units. Synertek 9,468 units.
Location
Fennimore, WI, United States
Initiation type
Voluntary: Firm initiated
Notification
Letter

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).

FDA source record · F-1015-2016

Data updated September 16, 2026. View official FDA data ↗

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