FDA recall record
Colostrum Powder, Dietary Supplement, Allergen statement: contains dairy. Colostrum (bovine) packaged in the following sizes and brand names: 1. PerCoBa Extra Edge Net Wei...
FDA classification. FDA Class I, II, and III are not the same as USDA FSIS classifications and are not a cross-agency safety score.
FDA listed a termination date of May 10, 2016. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
Colostrum Powder, Dietary Supplement, Allergen statement: contains dairy. Colostrum (bovine) packaged in the following sizes and brand names: 1. PerCoBa Extra Edge Net Weight 150 grams, UPC 90576-00099. 3,000 mg Colostrum (bovine) per 2 teaspoons. , 1800 Dodge Street, Fennimore, WI 53809; 2. PerCoBa Extra Edge Net Weight 250 grams, UPC 90576-00001. 3,000 mg Colostrum (bovine) per 2 teaspoons. ; 3.
8 ounces, UPC 09408-29292. 1,500 mg Colostrum (bovine) per 1 teaspoon. , Cheyenne, WY 82009.
Reason
The PerCoBa brand and Synertek brand Colostrum product labels should state contains milk.
Products involved
Product descriptions are copied from the FDA recall record. They are not a current catalog and are not automatically matched to WhoMadeMyFood product pages.
Colostrum Powder, Dietary Supplement, Allergen statement: contains dairy. Colostrum (bovine) packaged in the following sizes and brand names: 1. PerCoBa Extra Edge Net Weight 150 grams, UPC 90576-00099. 3,000 mg Colostrum (bovine) per 2 teaspoons. , 1800 Dodge Street, Fennimore, WI 53809; 2. PerCoBa Extra Edge Net Weight 250 grams, UPC 90576-00001. 3,000 mg Colostrum (bovine) per 2 teaspoons. ; 3.
8 ounces, UPC 09408-29292. 1,500 mg Colostrum (bovine) per 1 teaspoon. , Cheyenne, WY 82009.
Code information listed by FDA
250 gram jar Lots: 627-30, 628-30, 628-31, 630-31, 632-30, 633-30, 633-31, 635-30, 635-35, 636-30, 637-30, 637-31, 638-30, 638-31, 639-30, 639-31, 639-32, 641-30, 642-30, 644-30, 644-31, 646-30. 8 ounce jar Lots: 627-30, 628-30, 628-31, 630-31, 632-30, 633-30, 633-31, 635-30, 635-35, 636-30, 637-30, 637-31, 638-30, 638-31, 639-30, 639-31, 639-32, 641-30, 642-30, 644-30, 644-31, 646-30
Distribution and firm information
Recalling firm listed by FDA: Immuno - Dynamics, Inc
Firm location listed by FDA: Fennimore, WI, United States
Distribution reported by FDA: 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).
Product quantity listed by FDA: 250 gram jars - 2,532 units. 150 gram jars - 68 units. 8.8 ounce jars - 11,008 units
Source
Source: U.S. Food and Drug Administration (FDA), openFDA food enforcement reports.
Official FDA openFDA food enforcement record
Identifying an FDA recall record does not imply FDA endorsement of WhoMadeMyFood. Methodology.