Colostrum Lozenges, Dietary Supplement, Colostrum (Bovine) 200mg. Allergen statement: contains…
Recalling firm: Immuno - Dynamics, Inc
The PerCoBa brand and Synertek brand Colostrum product labels should state contains milk.
Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: May 10, 2016.
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FDA code information
PerCoBa Lots: 627-20, 638-20. Synertek Lots: 627-20, 638-20.
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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.
Original FDA recall reason
The PerCoBa brand and Synertek brand Colostrum product labels should state contains milk.
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).
Data updated September 16, 2026. View official FDA data ↗
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