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Recall company profile

Immuno - Dynamics, Inc. Recalls

Overview of recall records associated with Immuno - Dynamics, Inc., including dates, categories and classifications where available.

5recall records

Apr 13, 2016latest record date

Apr 13, 2016earliest record date

Recall history in this database

Classification mix: Class III: 4, Class II: 1.

FoodApr 13, 2016

Immuno - Dynamics Colostrum Powder, Dietary Supplement, Allergen statement recall — FDA F-1013-2016

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

Class IIIFDA: TerminatedImmuno - Dynamics, Inc.

FoodApr 13, 2016

Immuno - Dynamics PerCoBa Colostrum Capsules, Dietary Supplement, Colostrum recall — FDA F-1014-2016

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

Class IIIFDA: TerminatedImmuno - Dynamics, Inc.

FoodApr 13, 2016

Immuno - Dynamics PerCoBa 1, Colostral Whey, Dietary Supplement, Colostral Whey recall — FDA F-1016-2016

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

Class IIFDA: TerminatedImmuno - Dynamics, Inc.

FoodApr 13, 2016

Immuno - Dynamics Colostrum Lozenges, Dietary Supplement, Colostrum recall — FDA F-1015-2016

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

Class IIIFDA: TerminatedImmuno - Dynamics, Inc.

FoodApr 13, 2016

Immuno - Dynamics PerCoBa Whey Protein Isolate with Colostrum, Dietary recall — FDA F-1017-2016

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

Class IIIFDA: TerminatedImmuno - Dynamics, Inc.

Understanding this recall history

This page summarizes recall records in which the official source identifies Immuno - Dynamics, Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.

Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.