FDA recall record
FE RedBell Pepper, Product Code 22760. 50 lb corrugated case with polyliner. Manufactured by: QualiTech, 318 Hazeltine Drive, Chaska, MN 55318 USA
FDA classification. FDA Class I, II, and III are not the same as USDA FSIS classifications and are not a cross-agency safety score.
FDA listed a termination date of September 13, 2017. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
FE RedBell Pepper, Product Code 22760. 50 lb corrugated case with polyliner. Manufactured by: QualiTech, 318 Hazeltine Drive, Chaska, MN 55318 USA
Reason
QualiTech has been notified by a supplier that they received material with the potential presence of E. coli O121 bacteria.
Products involved
Product descriptions are copied from the FDA recall record. They are not a current catalog and are not automatically matched to WhoMadeMyFood product pages.
FE RedBell Pepper, Product Code 22760. 50 lb corrugated case with polyliner. Manufactured by: QualiTech, 318 Hazeltine Drive, Chaska, MN 55318 USA
Code information listed by FDA
Lot: 31645, 31643
Distribution and firm information
Recalling firm listed by FDA: QualiTech, Inc
Firm location listed by FDA: Chaska, MN, United States
Distribution reported by FDA: AZ, CA, GA, ID, IL, IN, MI, MN, TX, WA. Outside the US to include: Canada.
Product quantity listed by FDA: 400 lbs.
Source
Source: U.S. Food and Drug Administration (FDA), openFDA food enforcement reports.
Official FDA openFDA food enforcement record
Identifying an FDA recall record does not imply FDA endorsement of WhoMadeMyFood. Methodology.