Colostrum Lozenges — Class III food recall F-1015-2016
Terminated recall by Immuno - Dynamics, Inc, reported 2016-04-13, distributed nationwide. The PerCoBa brand and Synertek brand Colostrum product labels should state contains milk.
| Recall number | F-1015-2016 |
|---|---|
| Product type | Food |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Immuno - Dynamics, Inc, Fennimore, WI, United States |
| Recall initiated | 2015-11-10 |
| Classified | 2016-04-04 |
| Reported by FDA | 2016-04-13 |
| Terminated | 2016-05-10 |
| Distributed | Nationwide (US) |
| Countries outside the US | AU, CA, DE, FI, FR, GB, GR, IE, IL, IT, LK, MX, MY, NL, NO, SE, SG, TH, TR |
| Reason classes | labeling |
| Lot numbers | 627-20, 638-20 |
Product
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.
Reason for recall
The PerCoBa brand and Synertek brand Colostrum product labels should state contains milk.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/F-1015-2016. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.