Medium Battered Jo-Jo Wedges / 00126 (5 lb bags)
FDA Recall #F-3441-2017 — Class II — June 20, 2017
Recall Summary
| Recall Number | F-3441-2017 |
| 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 Battered Jo-Jo Wedges / 00126 (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
4897 cases
Product Codes / Lot Numbers
Lot Codes: 161219101000126 161219102000126 161219103000126 161219104000126 161219105000126 161219106000126 161219107000126 161219108000126 161219109000126 161219110000126 161219111000126 161219113000126 161219114000126 161219115000126 161219116000126 170117201000126 170117202000126 170117203000126 170117204000126 170117205000126 170117206000126 170117207000126 170117208000126 170204101000126 170204102000126 170204103000126 170204104000126 170204105000126 170204106000126 170204107000126 170204108000126 170204109000126 170204110000126 170204111000126 170204112000126 170204113000126 170204114000126 170204115000126 170204116000126 170204201000126 170204202000126 170204203000126 170204204000126 170204205000126 170204206000126 170204207000126 170204208000126 170204209000126 170204210000126 170204211000126 170204212000126 170204213000126 170204214000126 170204215000126 170204216000126 170204217000126 170217201000126 170217202000126 170217203000126 170217204000126 170217206000126 170217208000126 170217209000126 170217210000126 170217211000126 170217212000126 170217213000126 170217214000126 170217215000126 170217216000126 170217217000126 170217219000126 170217220000126 170405101000126 170405102000126 170405103000126 170405104000126 170405105000126 170405106000126 170405107000126 170405108000126 170405109000126 170405110000126 170405111000126 170405112000126 170405113000126 170405114000126 170405115000126 170405116000126 170405117000126 170405118000126
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.