Medium Seasoned/Battered Jo-Jo Wedges / 00129 (5 lb bags)
FDA Recall #F-3436-2017 — Class II — June 20, 2017
Recall Summary
| Recall Number | F-3436-2017 |
| Date Initiated | June 20, 2017 |
| Classification | Class II |
| Status | Terminated |
| Type | Voluntary: Firm initiated |
| Product Type | Food |
Recalling Firm
| Firm | Penobscot McCrum LLC |
| Location | Belfast, ME |
Product Description
Medium Seasoned/Battered Jo-Jo Wedges / 00129 (5 lb bags)
Reason for Recall
Product may contain undeclared milk.
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
LA, PA, OH, IL, KY, IN, TN, TX, FL, SC, CO, CA, AR, NC, MN, ME, AL, MI, VA, NY, IA, NJ, MA, MS, GA, WI
Product Quantity
5782 cases
Product Codes / Lot Numbers
Lot Codes: 161212101000129 161212103000129 161212102000129 161212104000129 161212105000129 161212106000129 161212107000129 161212108000129 161212109000129 161212110000129 161212111000129 161212112000129 161212113000129 161212114000129 161212115000129 161212116000129 161212117000129 161212118000129 161212119000129 161212120000129 161219201000129 161219202000129 161219203000129 161219204000129 161219205000129 161219206000129 161219207000129 161219208000129 161219209000129 161219210000129 161219211000129 161219212000129 161219213000129 161219214000129 161219215000129 161219216000129 161219217000129 161219218000129 170217101000129 170217102000129 170217103000129 170217104000129 170217105000129 170217106000129 170217107000129 170217108000129 170217109000129 170217110000129 170217111000129 170217112000129 170217113000129 170217114000129 170217115000129 170217116000129 170301201000129 170301202000129 170301203000129 170301204000129 170301205000129 170301206000129 170301207000129 170301208000129 170301209000129 170301210000129 170301211000129 170301212000129 170301213000129 170301214000129 170301215000129 170301216000129 170301217000129 170308105000129 170308106000129 170308109000129 170308110000129 170308115000129 170308116000129 170308118000129 170308119000129 170308121000129 170308201000129 170308203000129 170308204000129 170308205000129 170308206000129 170308207000129 170308208000129 170308209000129 170308210000129 170308212000129 170308214000129 170308215000129 170308216000129 170308217000129 170308218000129 170308220000129 170308221000129 170308222000129 170605101000129 170605102000129 170605103000129 170605104000129
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.
If you have a food allergy and consumed the recalled product, monitor yourself closely for allergic reaction symptoms — including hives, swelling, difficulty breathing, nausea, vomiting, or anaphylaxis. If you experience any symptoms, seek medical attention immediately. For anaphylaxis (severe allergic reaction with difficulty breathing, rapid heartbeat, or loss of consciousness), call 911 and use an epinephrine auto-injector (EpiPen) if available. Stop consuming the product and check all products from the same manufacturer for similar labeling issues, as undeclared allergens sometimes affect multiple products from the same production facility.
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.