Jody's Gourmet Popcorn, Fabulous Fudge Chocolate Walnut, net weight 8 oz. , ...

FDA Recall #F-0622-2016 — Class II — December 3, 2015

Recall Summary

Recall NumberF-0622-2016
Date InitiatedDecember 3, 2015
ClassificationClass II
StatusTerminated
TypeVoluntary: Firm initiated
Product TypeFood

Recalling Firm

FirmJody's Gourmet Popcorn
LocationVirginia Beach, VA

Product Description

Jody's Gourmet Popcorn, Fabulous Fudge Chocolate Walnut, net weight 8 oz. , one unit per package, packed in clear clamshell, expiration date 12/22/15

Reason for Recall

Jody's Inc. received a few notifications from people who bought the fudge as part of a school fund raiser that the fudge had mold on it. The expiration date of the fudge is 12/22/15, and it should not be growing mold yet. The firm immediately recalled the fudge.

Classification

Class II — A situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.

Distribution Pattern

The fudge was distributed in fulfillment of seven school fundraising projects. The fudge was delivered to the schools from October 26, 2015 through November 12, 2015. There were no foreign accounts, and there were no US government accounts (military or civilian). The schools that received the product, and the number of units delivered, are listed below, along with the school organizer, who we have alerted to the recall: Portsmouth Christian School - 52 units 3214 Elliott Ave Portsmouth, Va 23702 Jan Collins [email protected] Hodges Manor ES  19 units 1201 Cherokee Rd Portsmouth, Va 23701 Vallery Theus [email protected] JEJ Moore MS  39 units 11455 Prince George Dr Disputanta, Va 23842 Tracy Brunner [email protected] Moyock MS  11 units 216 Survey Rd Moyock, NC 27958 Elizabeth Sweeney [email protected] Lynnhaven ES  2 units 210 Dillon Dr. Va. Beach, Va 23452 Laurent Bracey [email protected] Simonsdale ES PTA  29 units 4841 Clifford Street Portsmouth, VA 23707 Amy Beaulier [email protected] Glen Allen High School 10700 Staples Mill Rd. Glen Allen, VA 23060 Sherry Ingram Note: The distributor, Sterling Ideas Unlimited handled communication with this school.

Product Quantity

215 packages of fudge were produced and distributed

Product Codes / Lot Numbers

Batch Numbers: 1528802-F and 1528801-F

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.

In most cases, yes. Retailers are typically notified to accept returns of recalled products and issue refunds, regardless of whether you have a receipt. Check with the store where you purchased the item. Some manufacturers also offer direct refunds — contact the recalling firm using the information in the official recall notice. If you purchased the product online, contact the retailer's customer service with your order number. In either case, you generally do not need original packaging, though retaining the product label with the lot code or UPC can speed up the process.

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.