Colostrum Lozenges recalled over undeclared allergens
- Recall date
- November 10, 2015
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Official notice title
- Immuno - Dynamics, Inc recalls Colostrum Lozenges, Dietary Supplement, Colostrum (Bovine) 200mg. Allergen statement: contains dairy. Packaged in the f…
- Recall number
- F-1015-2016
- FDA classification
- Class III
- Brand / firm
- Immuno - Dynamics, Inc
- Sold / 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).
Why it was recalled
The PerCoBa brand and Synertek brand Colostrum product labels should state contains milk.
Class III means the product violates regulations but is not likely to cause harm.
What 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.
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