FE Jalapeno 709 — Class I food recall F-0200-2017
Terminated recall by QualiTech, Inc, reported 2016-10-26, distributed in AZ, CA, GA, ID, IL, IN, MI, MN…. Quali Tech has been notified by a supplier that they received material with the potential presence of E. coli
| Recall number | F-0200-2017 |
|---|---|
| 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 | 3,200 pounds |
| Reason classes | microbial contamination |
| Pathogens | e coli |
| Lot numbers | 31504, 31756 |
Product
FE Jalapeno 709, Product Code 22709. 50 lb corrugated case with polyliner. Manufactured by: Quali Tech, 318 Hazel tine Drive, Chasma, MN 55318 USA
Reason for recall
Quali Tech has been notified by a supplier that they received material with the potential presence of E. coli O 121 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-0200-2017. 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.