Recalls / Class I
Class IF-0196-2017
Class I— FDA's most serious classification, issued when there is a reasonable probability that consumption of or exposure to the product will cause serious adverse health consequences or death.
Product
FE RedBell Pepper 339, Product Code 22339. 50 lb corrugated case with polyliner. Manufactured by: QualiTech, 318 Hazeltine Drive, Chaska, MN 55318 USA
- Type
- Food
- Affected lot / code info
- Lot codes: 31476, 31802
- Quantity
- 6,000 lbs.
Why it was recalled
QualiTech has been notified by a supplier that they received material with the potential presence of E. coli O121 bacteria.
Recalling firm
- Firm
- QualiTech, Inc
- Notification channel
- Type
- Voluntary: Firm initiated
- Address
- 318 Lake Hazeltine Dr, N/A, Chaska, Minnesota 55318-1034
Distribution
- Distribution pattern
- AZ, CA, GA, ID, IL, IN, MI, MN, TX, WA. Outside the US to include: Canada.
Timeline
- Recall initiated
- 2016-07-05
- FDA classified
- 2016-10-19
- Posted by FDA
- 2016-10-26
- Terminated
- 2017-09-13
- Status
- Terminated
Source: openFDA Food Enforcement endpoint. Recall record F-0196-2017. The FDA issues recall classifications as health-hazard assessments, not legal findings.