FDA Food recall F-1015-2016
Colostrum Lozenges, Dietary Supplement, Colostrum (Bovine) 200mg
- FDA Food
- Class III
- terminated
- Published 2016-04-13
On 2016-04-13 the FDA classified a Class III recall of Colostrum Lozenges, Dietary Supplement, Colostrum (Bovine) 200mg by Immuno Dynamics, citing the PerCoBa brand and Synertek brand Colostrum product labels should state contains milk.
Read the official FDA Food notice
| Agency | FDA Food |
|---|---|
| Recall number | F-1015-2016 |
| Classification | Class III |
| Status | terminated |
| Initiated | 2015-11-10 |
| Published | 2016-04-13 |
| Last updated | 2026-09-13 11:49 UTC |
| Company | Immuno Dynamics |
| Distribution | US |
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
The PerCoBa brand and Synertek brand Colostrum product labels should state contains milk.
Identifiers
| code_info | PerCoBa Lots: 627-20, 638-20. Synertek Lots: 627-20, 638-20. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:49 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1015-2016%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.