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

Colostrum Lozenges 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 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.

Quantity: PerCoBa 3,310 units. Synertek 9,468 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.

PerCoBa Lots: 627-20, 638-20. Synertek Lots: 627-20, 638-20.

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-1015-2016 · 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

Colostrum Powder Dietary Supplement

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

Immuno - Dynamics, Inc Nationwide F-1013-2016
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 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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