FDA recall record
Sysco X-Large Jo-Jo Wedges / 7641749 (5 lb bags)
FDA classification. FDA Class I, II, and III are not the same as USDA FSIS classifications and are not a cross-agency safety score.
FDA listed a termination date of November 3, 2017. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
Sysco X-Large Jo-Jo Wedges / 7641749 (5 lb bags)
Reason
Product may contain undeclared milk.
Products involved
Product descriptions are copied from the FDA recall record. They are not a current catalog and are not automatically matched to WhoMadeMyFood product pages.
Sysco X-Large Jo-Jo Wedges / 7641749 (5 lb bags)
Code information listed by FDA
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
Distribution and firm information
Recalling firm listed by FDA: Penobscot McCrum LLC
Firm location listed by FDA: Belfast, ME, United States
Distribution reported by FDA: 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 listed by FDA: 7307 cases
Source
Source: U.S. Food and Drug Administration (FDA), openFDA food enforcement reports.
Official FDA openFDA food enforcement record
Identifying an FDA recall record does not imply FDA endorsement of WhoMadeMyFood. Methodology.