FI Dry Blueberry / Strawberry Blend
Reason QualiTech has been notified by a supplier that they received material with the potential presence of E. coli O121 bacteria.
FE Green Bell Pepper 338 recall
Recalled by QualiTech, Inc · Chaska, MN, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
QualiTech has been notified by a supplier that they received material with the potential presence of E. coli O121 bacteria.
Pathogen: E. coli
Shiga toxin-producing E. coli (such as O157:H7) can cause severe illness and kidney failure.
The most serious food recalls: a contaminated product can cause outbreaks, hospitalisations and deaths, especially for pregnant people, young children, older adults and anyone with a weakened immune system. All bacteria & viruses recalls.
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
Quantity: 300 lbs.
Food: Spices & seasonings
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
Lot 31483
Where it was sold
Arizona California Georgia Idaho Illinois Indiana Michigan Minnesota Texas Washington
FDA's distribution note: AZ, CA, GA, ID, IL, IN, MI, MN, TX, WA. Outside the US to include: Canada.
Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- QualiTech, Inc
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Jul 5, 2016
- In FDA report of
- Oct 26, 2016
- Terminated
- Sep 13, 2017
- FDA recall number
- F-0195-2017 · event 74650
- Official record
- FDA enforcement report search
Also recalled with it (17 more products)
FDA files each product of one recall action separately; these share the same FDA event.
FE Carrot 281 Product Code 22281
Reason QualiTech has been notified by a supplier that they received material with the potential presence of E. coli O121 bacteria.
FE Bacon 286 Product Code 22286
Reason QualiTech has been notified by a supplier that they received material with the potential presence of E. coli O121 bacteria.
FE Jalapeno 321A
Reason QualiTech has been notified by a supplier that they received material with the potential presence of E. coli O121 bacteria.
FE RedBell Pepper 339
Reason QualiTech has been notified by a supplier that they received material with the potential presence of E. coli O121 bacteria.
FE Spinach 352 Product Code 22352
Reason QualiTech has been notified by a supplier that they received material with the potential presence of E. coli O121 bacteria.
FE Cheddar Cheese
Reason QualiTech has been notified by a supplier that they received material with the potential presence of E. coli O121 bacteria.
FE Red Bell Pepper
Reason QualiTech has been notified by a supplier that they received material with the potential presence of E. coli O121 bacteria.
FE Jalapeno 709 Product Code 22709
Reason Quali Tech has been notified by a supplier that they received material with the potential presence of E. coli O 121 bacteria.
FE Rainbow Blend 714
Reason QualiTech has been notified by a supplier that they received material with the potential presence of E. coli O121 bacteria.
FE Green Bell Pepper
Reason QualiTech has been notified by a supplier that they received material with the potential presence of E. coli O121 bacteria.
FE RedBell Pepper
Reason QualiTech has been notified by a supplier that they received material with the potential presence of E. coli O121 bacteria.
Showing 12 of 17.