FE RedBell Pepper, Product Code 22760. 50 lb corrugated case with polyliner....
FDA Recall #F-0203-2017 — Class I — July 5, 2016
Recall Summary
| Recall Number | F-0203-2017 |
| Date Initiated | July 5, 2016 |
| Classification | Class I |
| Status | Terminated |
| Type | Voluntary: Firm initiated |
| Product Type | Food |
Recalling Firm
| Firm | QualiTech, Inc |
| Location | Chaska, MN |
Product Description
FE RedBell Pepper, Product Code 22760. 50 lb corrugated case with polyliner. Manufactured by: QualiTech, 318 Hazeltine Drive, Chaska, MN 55318 USA
Reason for Recall
QualiTech has been notified by a supplier that they received material with the potential presence of E. coli O121 bacteria.
Classification
Class I — A situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Distribution Pattern
AZ, CA, GA, ID, IL, IN, MI, MN, TX, WA. Outside the US to include: Canada.
Product Quantity
400 lbs.
Product Codes / Lot Numbers
Lot: 31645, 31643
What Should You Do?
Stop consuming this product immediately. Check your home for the recalled item and dispose of it safely. If you experienced a health issue after consuming this product, contact your doctor and report it to the FDA MedWatch.
Frequently Asked Questions
Stop consuming the product immediately and do not donate or give it to others. Check the recall notice above for specific disposal or return instructions. Many food recalls ask you to throw the product away and retain the packaging for a possible refund from the retailer. If you purchased it online, check your order history — some retailers send recall notifications directly to customers. You do not need a receipt to report an issue or seek a refund; the fact of purchase is typically sufficient.
Certain strains — particularly E. coli O157:H7 and other Shiga toxin-producing E. coli (STEC) — can cause severe illness. Symptoms typically begin 3 to 4 days after exposure and include severe stomach cramps, diarrhea (often bloody), and vomiting. Most people recover within 5 to 7 days. However, about 5 to 10% of those with STEC infection develop Hemolytic Uremic Syndrome (HUS), a type of kidney failure that can be life-threatening, especially in children under 5 and the elderly. Seek medical attention if you develop bloody diarrhea or symptoms worsen significantly after a few days.
Report foodborne illnesses and adverse food reactions to the FDA through the MedWatch Safety Reporting Portal at FDA.gov, or by calling 1-800-332-1088. You can also report issues directly to the FDA's Safety Reporting Portal at SafetyReporting.hhs.gov. If you believe there is an immediate public health risk, contact your local health department. Your report helps the FDA identify contamination patterns, initiate recalls faster, and protect other consumers from the same hazard. Include as much detail as possible: the product name, lot code, purchase date and location, and a description of your symptoms or findings.
The FDA assigns a status to each recall action throughout its lifecycle. "Ongoing" means the recall is active — the firm is still working to remove the product from commerce and notify consumers. "Completed" means the recall strategy has been implemented and the FDA has determined that the recalling firm has taken all appropriate steps to remove the product. "Terminated" means the FDA has reviewed the results and concluded the recall is complete. Even if a recall is marked as completed or terminated, you should still discard any recalled products you find at home — the recall status refers to the firm's compliance actions, not the safety of product still in consumers' possession.