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-3441-2017

Event ID

77477

Status

Terminated

Classification

Class II

Company

Penobscot McCrum LLC

Product description

Medium Battered Jo-Jo Wedges / 00126 (5 lb bags)

Quantity

4897 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: 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

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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