Sysco X-Large Jo-Jo Wedges / 7641749 (5 lb bags)
FDA Recall #F-3439-2017 — Class II — June 20, 2017
Recall Summary
| Recall Number | F-3439-2017 |
| 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
Sysco X-Large Jo-Jo Wedges / 7641749 (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
7307 cases
Product Codes / Lot Numbers
Lot Codes: 170110101641749 170110102641749 170110103641749 170110104641749 170110105641749 170110106641749 170110107641749 170110108641749 170110109641749 170110110641749 170110111641749 170110112641749 170110113641749 170110114641749 170110115641749 170110116641749 170110117641749 170110201641749 170110202641749 170110203641749 170110204641749 170202101641749 170202102641749 170202103641749 170202104641749 170202105641749 170202107641749 170202108641749 170202201641749 170202202641749 170202203641749 170202204641749 170202205641749 170202206641749 170214101641749 170214102641749 170214103641749 170214104641749 170214105641749 170214107641749 170214108641749 170214109641749 170214201641749 170214202641749 170214203641749 170214204641749 170214205641749 170228201641749 170228202641749 170228203641749 170228204641749 170228205641749 170228206641749 170228207641749 170228208641749 170228209641749 170228210641749 170228211641749 170228212641749 170228213641749 170228214641749 170228215641749 170228215641749 170316102641749 170316104641749 170316105641749 170316106641749 170316201641749 170316202641749 170316203641749 170316204641749 170316205641749 170316206641749 170316207641749 170323201641749 170323202641749 170323203641749 170323204641749 170323205641749 170323206641749 170323207641749 170323208641749 170323209641749 170323210641749 170323211641749 170323212641749 170323213641749 170323214641749 170323215641749 170323216641749 170323217641749 170406101641749 170406102641749 170406103641749 170406104641749 170406105641749 170406106641749 170406107641749 170406108641749 170406109641749 170406110641749 170406111641749 170406112641749 170406113641749 170406114641749 170406115641749 170413101641749 170413104641749 170413105641749 170413106641749 170413107641749 170413108641749 170413109641749 170413113641749 170413114641749 170501103641749 170501104641749 170501106641749 170501107641749 170501108641749 170501109641749 170501110641749 170501111641749 170501204641749 170501206641749 170519104641749 170519106641749 170519107641749 170519108641749 170519201641749 170524108641749 170524112641749 170524113641749 170524114641749 170524201641749 170524203641749
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.