FE Rainbow Blend — Class I food recall F-0205-2017
Terminated recall by QualiTech, Inc, reported 2016-10-26, distributed in AZ, CA, GA, ID, IL, IN, MI, MN…. QualiTech has been notified by a supplier that they received material with the potential presence of E. coli O
| Recall number | F-0205-2017 |
|---|---|
| Product type | Food |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | QualiTech, Inc, Chaska, MN, United States |
| Recall initiated | 2016-07-05 |
| Classified | 2016-10-19 |
| Reported by FDA | 2016-10-26 |
| Terminated | 2017-09-13 |
| Distributed | AZ, CA, GA, ID, IL, IN, MI, MN, TX, WA |
| Countries outside the US | CA |
| Quantity | 1,400 pounds |
| Reason classes | microbial contamination |
| Pathogens | e coli |
| Lot numbers | 31950 |
Product
FE Rainbow Blend, Product Code 22795. 50 lb corrugated case with polyliner. Manufactured by: QualiTech, 318 Hazeltine Drive, Chaska, MN 55318 USA
Reason for recall
QualiTech has been notified by a supplier that they received material with the potential presence of E. coli O121 bacteria.
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-0205-2017. 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.