Food City Colby Jack Cheese, 12 oz. package; also sold in random weight sizes...
FDA Recall #F-1662-2017 — Class I — February 16, 2017
Recall Summary
| Recall Number | F-1662-2017 |
| Date Initiated | February 16, 2017 |
| Classification | Class I |
| Status | Terminated |
| Type | Voluntary: Firm initiated |
| Product Type | Food |
Recalling Firm
| Firm | Lakeview Cheese Co Llc |
| Location | Las Vegas, NV |
Product Description
Food City Colby Jack Cheese, 12 oz. package; also sold in random weight sizes (Bashas' brand name) Also sold in 4/13# with Lakeview name; Banquet Baby Colby Jack RW Wheel 18/2# : Colby Jack LH 20/1# CW Banquet; Colby Jk Longhorn Cheese 16 oz. Yoke's Fresh Market 20# case and Longhorn Colby Jack RQ EW case 36# no label for Bashas' Longhorn is just a different shape, same recipe. Banquet is a Lakeview brand name.
Reason for Recall
Firm was notified by supplier that cheese supplied to Lakeview from September 1, 2016 through January 27, 2017 is being recalled due to the potential of Listeria monocytogenes. contamination.
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, UT, NV, WA, OR.
Product Quantity
355,477.90 pounds of cheese (all varieties)
Product Codes / Lot Numbers
All product received by Lakeview between September 1, 2016 and January 27, 2017. Lakeview Codes: 1119 Co-Jack LH 4/13#; 4356 Colby/Jack LH 48/12 oz.; 4359 Longhorn Colby/Jack RW EW case 36# No Label; 5537 Co Jack LH 20/1# CW Banquet Label; 622415 LH Colby/Jack 4/13 # - Bashas'.
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.
Listeria monocytogenes is one of the most serious foodborne pathogens. Unlike most bacteria, Listeria can grow at refrigerator temperatures (below 40°F), meaning refrigerating a contaminated product does not stop the risk. Symptoms can appear 1 to 4 weeks after eating contaminated food and may include fever, muscle aches, headache, stiff neck, confusion, and loss of balance. Listeriosis is particularly dangerous for pregnant women — infection can cause miscarriage, stillbirth, or premature delivery. If you consumed this recalled product and are in a high-risk group (pregnant, elderly, or immunocompromised), contact your doctor immediately even if you feel well.
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.