FE Green Bell Pepper 338 recalled over E. coli risk

Recall date

July 5, 2016

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Official notice title

QualiTech, Inc recalls FE Green Bell Pepper 338, Product Code 22338. 50 lb corrugated case with polyliner. Manufactured by: QualiTech, 318 Haz…

Recall number

F-0195-2017

FDA classification

Class I

Brand / firm

QualiTech, Inc

Sold / distributed

AZ, CA, GA, ID, IL, IN, MI, MN, TX, WA. Outside the US to include: Canada.

Why it was recalled

QualiTech has been notified by a supplier that they received material with the potential presence of E. coli O121 bacteria.

Class I is the FDA’s most serious recall level: there is a reasonable probability that using this product will cause serious harm or death.

What was recalled

FE Green Bell Pepper 338, Product Code 22338. 50 lb corrugated case with polyliner. Manufactured by: QualiTech, 318 Hazeltine Drive, Chaska, MN 55318 USA