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.
Reported: April 13, 2016 Initiated: November 10, 2015 #F-1015-2016
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.
Reason for Recall
The PerCoBa brand and Synertek brand Colostrum product labels should state contains milk.
Details
- Recalling Firm
- Immuno - Dynamics, Inc
- Units Affected
- PerCoBa 3,310 units. Synertek 9,468 units.
- Distribution
- 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).
- Location
- Fennimore, WI
Frequently Asked Questions
What product was recalled? ▼
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.. Recalled by Immuno - Dynamics, Inc. Units affected: PerCoBa 3,310 units. Synertek 9,468 units..
Why was this product recalled? ▼
The PerCoBa brand and Synertek brand Colostrum product labels should state contains milk.
Which agency issued this recall? ▼
This recall was issued by the FDA Food on April 13, 2016. Severity: Low. Recall number: F-1015-2016.
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