Penobscot McCrum LLC Recall: Product may contain undeclared milk.

🇺🇸 United States

1. June 20, 2017 - Recall initiated
2. August 30, 2017 - Reported by source
3. November 3, 2017 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-3439-2017

Event ID

77477

Status

Terminated

Classification

Class II

Company

Penobscot McCrum LLC

Product description

Sysco X-Large Jo-Jo Wedges / 7641749 (5 lb bags)

Quantity

7307 cases

Reason

Product may contain undeclared milk.

Recall initiation date

June 20, 2017

Report date

August 30, 2017

Classification date

Not published in this source record

Termination date

November 3, 2017

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

UPC, lot, and code information

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

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

Letter

Source last updated

Not tracked separately from the Public Health Trace retrieval date below

Public Health Trace retrieval date

July 18, 2026 ET

Other products recalled under this same event

This recall shares FDA event ID 77477 with 9 other product entries in Public Health Trace.

Responsible company: Penobscot McCrum LLC

Other recalls from Penobscot McCrum LLC

A map highlighting the states named in the source's distribution description.

Distributed No data published

Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.

Distribution map

State	Distributed
Louisiana	1
Pennsylvania	1
Ohio	1
Illinois	1
Kentucky	1
Indiana	1
Tennessee	1
Texas	1
Florida	1
South Carolina	1
Colorado	1
California	1
Arkansas	1
North Carolina	1
Minnesota	1
Maine	1
Alabama	1
Michigan	1
Virginia	1
New York	1
Iowa	1
New Jersey	1
Massachusetts	1
Mississippi	1
Georgia	1
Wisconsin	1

States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace: July 18, 2026 ET

Frequently asked questions

What does a Class II mean?

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

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.

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