FE RedBell Pepper 339, Product Code 22339. 50 lb corrugated case with polyliner.
Recalling firm: QualiTech, Inc
QualiTech has been notified by a supplier that they received material with the potential presence of E. coli O121 bacteria.
Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Sep 13, 2017.
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FDA code information
Lot codes: 31476, 31802
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Full FDA record and distribution details
Original product description
FE RedBell Pepper 339, Product Code 22339. 50 lb corrugated case with polyliner. Manufactured by: QualiTech, 318 Hazeltine Drive, Chaska, MN 55318 USA
Extracted codes and context
| Type | Code / value | Context |
|---|---|---|
| lot | 31476 | Lot codes: 31476, 31802 |
| lot | 31802 | Lot codes: 31476, 31802 |
Original FDA recall reason
QualiTech has been notified by a supplier that they received material with the potential presence of E. coli O121 bacteria.
Recall details
- Recall number
- F-0196-2017
- Event ID
- 74650
- FDA status
- Terminated
- Initiated
- Jul 5, 2016
- Reported
- Oct 26, 2016
- Classified
- Oct 19, 2016
- Terminated
- Sep 13, 2017
- Quantity
- 6,000 lbs.
- Location
- Chaska, MN, United States
- Initiation type
- Voluntary: Firm initiated
- Notification
Where it was distributed
AZ, CA, GA, ID, IL, IN, MI, MN, TX, WA. Outside the US to include: Canada.
Data updated September 16, 2026. View official FDA data ↗
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