PlainRecalls
FDA Food Verify with FDA Food → Low Class III Terminated

PerCoBa Colostrum Capsules, Dietary Supplement, Colostrum (bovine) 1g. 120 capsules. UPC 90576-00011. Allergen statement: contains dairy. Distributed by: Immuno-Dynamics, Inc., 1800 Dodge Street, Fennimore, WI 53809.

Reported: April 13, 2016 Initiated: November 10, 2015 #F-1014-2016 662 units units

The recall

Immuno - Dynamics, Inc issued this low-severity FDA Food recall — The PerCoBa brand and Synertek brand Colostrum product labels should state contains milk..

Low
severity level
662 units
units affected
Class III
classification
April 13, 2016
reported

Sourced from official FDA Food enforcement records. Verify recall #F-1014-2016 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.

Recall Insight

This FDA Food action (record #F-1014-2016) was formally reported on April 13, 2016, with the manufacturer initiating the action on November 10, 2015. It is classified under Low severity (Class III), with a current status of Terminated. Immuno - Dynamics, Inc is listed as the recalling firm, operating out of Fennimore, WI. Federal records indicate 662 units units are affected.

The documented reason for this recall is: The PerCoBa brand and Synertek brand Colostrum product labels should state contains milk. Distribution data in the federal record shows the product reached: 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 Lank…. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.

To put this record in context, PlainRecalls indexes 83,949 recalls across the FDA, CPSC and NHTSA going back to 1995. Within the same product category, the database holds 6 closely related recalls, of which 6 were also issued by FDA Food. That clustering is a signal — repeated actions in a narrow category often indicate a systemic quality-control issue, a supplier-wide contamination, or a design defect that has propagated across product lines. This recall is roughly 10 years old; older recalls can remain relevant because many units enter resale, rental, and secondary-market channels where the original warning never reaches the end user. Always cross-check the recall number against the official agency page before relying on any summary.

Where this recall sits in the database

Severity2119858883High severity (most serious)Moderate severityLow severity
Where this recall sits in the database

Of 83,949 recalls in the database, 21,198 are high severity, 58,883 moderate, and 3,868 low. This recall is classified low severity.

Severity

Low

Units Affected

662 units

Related Recalls

6

6 from same agency

Product Description

PerCoBa Colostrum Capsules, Dietary Supplement, Colostrum (bovine) 1g. 120 capsules. UPC 90576-00011. Allergen statement: contains dairy. Distributed by: Immuno-Dynamics, Inc., 1800 Dodge Street, Fennimore, WI 53809.

Reason for Recall

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

Details

Recalling Firm
Immuno - Dynamics, Inc
Units Affected
662 units
Distribution
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).
Location
Fennimore, WI

Recall Profile

Structured summary of the FDA Food recall record
Attribute Value
Agency U.S. Food and Drug Administration
Severity class Low (Class III)
Status Terminated
Recall number F-1014-2016
Date reported April 13, 2016
Date initiated November 10, 2015
Recalling firm Immuno - Dynamics, Inc
Units affected 662 units
Distribution 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,…

Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.

Scale of Impact

662 units units affected — limited or regional distribution scale.

Regional (<10K units) ✓ This recall
Multi-state (10K – 100K units)
Large-scale (100K – 1M units)
Massive (≥1M units)

Bracket cutoffs follow federal recall-disclosure conventions; bar widths scale linearly within each bracket. Source: PlainRecalls analysis of U.S. Food and Drug Administration filings.

Frequently Asked Questions

What product was recalled?
PerCoBa Colostrum Capsules, Dietary Supplement, Colostrum (bovine) 1g. 120 capsules. UPC 90576-00011. Allergen statement: contains dairy. Distributed by: Immuno-Dynamics, Inc., 1800 Dodge Street, Fennimore, WI 53809.. Recalled by Immuno - Dynamics, Inc. Units affected: 662 units.
Why was this product recalled?
The PerCoBa brand and Synertek brand Colostrum product labels should state contains milk.
Which agency issued this recall?
This recall was issued by the FDA Food on April 13, 2016. Severity: Low. Recall number: F-1014-2016.
Where was the recalled product distributed?
Distribution: 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)..
How do I check if my product is affected by a recall?
Check the product description and recall number (F-1014-2016) against your product. Visit the official FDA Food website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
What are the health risks of consuming a recalled food product?
Recalled food products may contain contaminants, undeclared allergens, or harmful bacteria such as Salmonella, Listeria, or E. coli. Consuming these products can cause foodborne illness ranging from mild gastrointestinal symptoms to serious conditions requiring hospitalization. If you have consumed a recalled food product and experience symptoms, contact your healthcare provider and report to the FDA via MedWatch.

Recall Context

Product recalls are issued when a manufacturer, distributor, or federal agency determines that a product poses a safety risk to consumers. Recall severity varies based on the likelihood and degree of potential harm to consumers. Across PlainRecalls, we track 83,000+ recalls from FDA, CPSC, and NHTSA to help consumers stay informed and act quickly when safety issues arise.

Nearby Recalls in This Category

Other recalls in the same product category — useful for spotting patterns across the same defect class or manufacturer.

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Data Sources

Source: FDA, CPSC, and NHTSA federal recall databases. This recall: FDA Food, reported April 13, 2016.

  • Source: FDA — Food and Drug Administration, openFDA Enforcement API (food, drug, and medical device recalls)
  • Source: CPSC — Consumer Product Safety Commission Recalls API (consumer product recalls and hazards)
  • Source: NHTSA — National Highway Traffic Safety Administration Recalls API (vehicle safety recalls)

Recall information is sourced from official federal agency databases. Always verify recall details with the issuing agency for the most current status. This information is for research and awareness purposes only.

Source: Federal recall agencies (FDA, CPSC, NHTSA) Aggregated federal recall feeds Recall data normalized across FDA, CPSC and NHTSA feeds; severity classifications follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type).