B911 Kirkman Max Spectrum E — Class II food recall F-0792-2014
Terminated recall by National Enzyme Co, reported 2013-12-25, distributed nationwide. Firm is recalling dietary supplements containing a raw material which may contain >0.3 ppb chloramphenicol
| Recall number | F-0792-2014 |
|---|---|
| Product type | Food |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | National Enzyme Co, Forsyth, MO, United States |
| Recall initiated | 2013-10-30 |
| Classified | 2013-12-13 |
| Reported by FDA | 2013-12-25 |
| Terminated | 2015-03-03 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA, CN, GB, KR, MY, NO, SE, SK, TW |
| Quantity | 1,138 bottles |
| Lot numbers | 54255000 |
Product
B911 Kirkman Max Spectrum E, packaged unlabeled, 90-capsule bottles (SKU 54255);
Reason for recall
Firm is recalling dietary supplements containing a raw material which may contain >0.3 ppb 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-0792-2014. 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.