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Policy version 2026-07-21, effective July 21, 2026.
United States
TerminatedClass I
QualiTech has been notified by a supplier that they received material with the potential presence of E. coli O121 bacteria.
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| FE Green Bell Pepper 338, Product Code 22338. 50 lb corrugated case with polyliner. Manufactured by: QualiTech, 318 Hazeltine Drive, Chaska, MN 55318 USA | Not published in this source record | 300 lbs. | Lot 31483 |
This recall shares FDA event ID 74650 with 10 other product entries in Public Health Trace.
FDA Recall United States TerminatedTerminated: September 13, 2017Historical recordClass I
FDA Recall United States TerminatedTerminated: September 13, 2017Historical recordClass I
FDA Recall United States TerminatedTerminated: September 13, 2017Historical recordClass I
FDA Recall United States TerminatedTerminated: September 13, 2017Historical recordClass I
FDA Recall United States TerminatedTerminated: September 13, 2017Historical recordClass I
FDA Recall United States TerminatedTerminated: September 13, 2017Historical recordClass I
FDA Recall United States TerminatedTerminated: September 13, 2017Historical recordClass I
FDA Recall United States TerminatedTerminated: September 13, 2017Historical recordClass I
FDA Recall United States TerminatedTerminated: September 13, 2017Historical recordClass I
FDA Recall United States TerminatedTerminated: September 13, 2017Historical recordClass I
Responsible company: QualiTech, Inc
FDA Recall United States TerminatedTerminated: September 13, 2017Historical recordClass I
FDA Recall United States TerminatedTerminated: September 13, 2017Historical recordClass I
FDA Recall United States TerminatedTerminated: September 13, 2017Historical recordClass I
A map highlighting the states named in the source's distribution description.
Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.
| State | Distributed |
|---|---|
| Arizona | 1 |
| California | 1 |
| Georgia | 1 |
| Idaho | 1 |
| Illinois | 1 |
| Indiana | 1 |
| Michigan | 1 |
| Minnesota | 1 |
| Texas | 1 |
| Washington | 1 |
States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.
View FDA enforcement record -- the specific openFDA record this summary was built from.
This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.
According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.
The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.
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