LANTANA White Bean HUMMUS NET WT. 10 oz (283g)
FDA Recall #F-3362-2017 — Class I — June 17, 2017
Recall Summary
| Recall Number | F-3362-2017 |
| Date Initiated | June 17, 2017 |
| Classification | Class I |
| Status | Terminated |
| Type | Voluntary: Firm initiated |
| Product Type | Food |
Recalling Firm
| Firm | House Of Thaller Inc |
| Location | Knoxville, TN |
Product Description
LANTANA White Bean HUMMUS NET WT. 10 oz (283g)
Reason for Recall
The firm was notified by their ingredient supplier that the pine nuts may be contaminated with Listeria monocytogenes.
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
Product was shipped to the following states: AL, AZ, CA, CO, CT, FL, GA, IA, ID, IL, IN, LA, MA, MD, MI, MN, MO, NC, ND, NE, NJ, NY, OH, OK, OR, PA, SC, TX, UT, VA, WA & WI. Product was also shipped to Canada.
Product Quantity
39,942 cs/8/10 oz cups
Product Codes / Lot Numbers
Expiration & Lot Codes: USE BY 19 JUN 2017A W1704129, USE BY 20 JUN 2017A W1704138, USE BY 22 JUN 2017A W1704161, USE BY 22 JUN 2017A W1704164, USE BY 22 JUN 2017A W1704165, USE BY 29 JUN 2017A W1704253, USE BY 29 JUN 2017A W1704254, USE BY 29 JUN 2017A W1704257, USE BY 30 JUN 2017A W1704274, USE BY 30 JUN 2017A W1704275, USE BY 04 JUL 2017A W1704346, USE BY 06 JUL 2017A W1704365, USE BY 06 JUL 2017A W1704366, USE BY 12 JUL 2017A W1704403, USE BY 12 JUL 2017A W1705004, USE BY 15 JUL 2017A W1705041, USE BY 15 JUL 2017A W1705044, USE BY 15 JUL 2017A W1705045, USE BY 18 JUL 2017A W1705088, USE BY 24 JUL 2017A W1705175, USE BY 24 JUL 2017A W1705176, USE BY 24 JUL 2017A W1705177, USE BY 26 JUL 2017A W1705199, USE BY 26 JUL 2017A W1705200, USE BY 27 JUL 2017A W1705201, USE BY 27 JUL 2017A W1705203, USE BY 27 JUL 2017A W1705207, USE BY 02 AUG 2017A W1705306, USE BY 02 AUG 2017A W1705307, USE BY 03 AUG 2017A W1705315, USE BY 03 AUG 2017A W1705316, USE BY 05 AUG 2017A W1705335, USE BY 05 AUG 2017A W1705336, USE BY 09 AUG 2017A W1705390, USE BY 10 AUG 2017A W1705401, USE BY 10 AUG 2017A W1705402 & USE BY 15 AUG 2017A W1706065.
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.