Food Recall Check
Class III · Low risk Terminated Initiated Nov 10, 2015 (11 years ago)

Colostrum Powder Dietary Supplement recall

Recalled by Immuno - Dynamics, Inc · Fennimore, WI, United States

Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.

Why it was recalled

The PerCoBa brand and Synertek brand Colostrum product labels should state contains milk.

A label that does not match the product can hide an ingredient someone must avoid, or show a wrong use-by date. All labeling errors recalls.

What was recalled

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. 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.

Quantity: 250 gram jars - 2,532 units. 150 gram jars - 68 units. 8.8 ounce jars - 11,008 units

Food: Dietary supplements

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

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. 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

Where it was sold

Nationwide.

Puerto Rico

FDA's distribution note: 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).

Low risk, but check. Class III means the product is unlikely to make anyone ill but breaks an FDA rule, often a labeling one. If your package matches, the store will normally refund it. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm
Immuno - Dynamics, Inc
Initiated by
Voluntary: Firm initiated
Recall initiated
Nov 10, 2015
In FDA report of
Apr 13, 2016
Terminated
May 10, 2016
FDA recall number
F-1013-2016 · event 72665
Official record
FDA enforcement report search

Also recalled with it (4 more products)

FDA files each product of one recall action separately; these share the same FDA event.

Class III · Low risk Terminated Labeling

PerCoBa Colostrum Capsules

Reason The PerCoBa brand and Synertek brand Colostrum product labels should state contains milk.

Immuno - Dynamics, Inc Nationwide F-1014-2016
Class III · Low risk Terminated Labeling

Colostrum Lozenges Dietary Supplement

Reason The PerCoBa brand and Synertek brand Colostrum product labels should state contains milk.

Immuno - Dynamics, Inc Nationwide F-1015-2016
Class II · Moderate risk Terminated Labeling

PerCoBa 1 Colostral Whey

Reason The PerCoBa brand and Synertek brand Colostrum product labels should state contains milk.

Immuno - Dynamics, Inc Nationwide F-1016-2016

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