FDA recalls · F-1013-2016
Immuno - Dynamics, Inc recall
- FoodColostrum 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. Immuno-Dynamics, Inc., 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. Immuno-Dynamics, Inc., 1800 Dodge Street, Fennimore, WI 53809.; 3. Synertek Balanced Pure, 8.8 ounces, UPC 09408-29292. 1,500 mg Colostrum (bovine) per 1 teaspoon. Distributed by Synertek Colostrum, Inc., Cheyenne, WY 82009.
- ReasonThe PerCoBa brand and Synertek brand Colostrum product labels should state contains milk.
- ClassClass III: the food is unlikely to cause health problems
- StatusClosed by FDA, ended 2016-05-10
- DatesFirm started it 2015-11-10. In FDA's enforcement report 2016-04-13.
- Sold inNationwide 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).
- Amount250 gram jars - 2,532 units. 150 gram jars - 68 units. 8.8 ounce jars - 11,008 units
- Codes250 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. 150 gram Jar Lots: 642-100 8.8 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
- FirmImmuno - Dynamics, Inc, Fennimore, WI · Voluntary: Firm initiated
Products we list
None. We tie a recall to a product only by a barcode printed in the recall, and this one names none we list. That does not mean the recalled food is missing from our listings.
From FDA's enforcement report, via openFDA (CC0): raw data for this recall. FDA's own Enforcement Report search finds it by its number, F-1013-2016. Class meanings: FDA.