Digest Ultra — Class II food recall F-1461-2014
Terminated recall by Health Wright Products Inc, reported 2014-02-05, distributed in CA, FL, OR, UT. Dietary supplement products are recalled because they were made from ingredient that was contaminated with Chl
| Recall number | F-1461-2014 |
|---|---|
| Product type | Food |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Health Wright Products Inc, Clackamas, OR, United States |
| Recall initiated | 2013-10-25 |
| Classified | 2014-01-30 |
| Reported by FDA | 2014-02-05 |
| Terminated | 2015-03-02 |
| Distributed | CA, FL, OR, UT |
| Countries outside the US | MX |
| Lot numbers | 01/12, 03/12, 03/13, 06/12, 06/14, 08/13, 10/14, 10190112, 10190312, 10190313, 10191112, 1019A0811, 11/12, 1207408, 1217703, 20190313, 20190612, 20191012, MFG-03/12 |
| Expiration dates | 2015-02 |
Product
Digest Ultra, dietary supplement, packaged 56 capsules per bottle or distributed in bulk, sold under brand YOR. Product distributed OUTSIDE the US has Spanish label.
Reason for recall
Dietary supplement products are recalled because they were made from ingredient that was contaminated with Chloramphenicol.
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-1461-2014. 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.