CLASS II Food recall · Reported 13 Apr 2016 · FDA Enforcement Report
PerCoBa 1, Colostral Whey, Dietary Supplement recalled
Immuno - Dynamics is recalling PerCoBa 1, Colostral Whey, Dietary Supplement, Colostral Whey Protein 4%. Net Contents, distributed nationwide in the US. The recall was initiated on 10 Nov 2015 and the FDA has classified it as Class II.
Check your package
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Recall details
- Recall number
- F-1016-2016
- FDA event ID
- 72665
- Recalling firm
- Immuno - Dynamics, Fennimore, WI
- Brand
- PerCoBa
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 10 Nov 2015
- FDA classified
- 4 Apr 2016
- Reported
- 13 Apr 2016
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Other Reasons
- Product category
- Protein Powder
Timeline
| 10 Nov 2015 | Recall initiated by company | |
| 4 Apr 2016 | Classified by FDA | +146 days |
| 13 Apr 2016 | Published in enforcement report | +9 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
The PerCoBa brand and Synertek brand Colostrum product labels should state contains milk.
Product as listed by the FDA
PerCoBa 1, Colostral Whey, Dietary Supplement, Colostral Whey Protein 6.4%. Net Contents: 4 oz. Immuno-Dynamics, Inc. , PO Box 544 Perry, Iowa 50220
Where it was distributed
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).
Questions about this recall
Is PerCoBa 1, Colostral Whey, Dietary Supplement, Colostral Whey Protein 4%. Net Contents recalled?
Yes. Immuno - Dynamics recalled PerCoBa 1, Colostral Whey, Dietary Supplement, Colostral Whey Protein 4%. Net Contents on 10 Nov 2015. The recall is Class II and its status is Terminated. Recall number F-1016-2016.
Why was it recalled?
The PerCoBa brand and Synertek brand Colostrum product labels should state contains milk.
Which lots are affected?
Lots: 477, 479, 481, 484.
Where was it sold?
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).
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
More recalls from Immuno - Dynamics
All 5| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Food | CLASS III | PerCoBa Whey Protein Isolate with Colostrum, Dietary Supplement recalledPerCoBa Whey | Immuno - Dynamics | Other | Nationwide |
| Food | CLASS III | Colostrum Lozenges, Dietary Supplement, Colostrum (Bovine) 200mg recalledColostrum Lozenges | Immuno - Dynamics | Undeclared Allergens | Nationwide |
| Food | CLASS III | PerCoBa Colostrum Capsules, Dietary Supplement, Colostrum (bovine) recalledPerCoBa Colostrum | Immuno - Dynamics | Undeclared Allergens | Nationwide |
| Food | CLASS III | Colostrum Powder, Dietary Supplement, Allergen statement recalledColostrum | Immuno - Dynamics | Undeclared Allergens | Nationwide |
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