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-3436-2017

Event ID

77477

Status

Terminated

Classification

Class II

Company

Penobscot McCrum LLC

Product description

Medium Seasoned/Battered Jo-Jo Wedges / 00129 (5 lb bags)

Quantity

5782 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: 161212101000129 161212103000129 161212102000129 161212104000129 161212105000129 161212106000129 161212107000129 161212108000129 161212109000129 161212110000129 161212111000129 161212112000129 161212113000129 161212114000129 161212115000129 161212116000129 161212117000129 161212118000129 161212119000129 161212120000129 161219201000129 161219202000129 161219203000129 161219204000129 161219205000129 161219206000129 161219207000129 161219208000129 161219209000129 161219210000129 161219211000129 161219212000129 161219213000129 161219214000129 161219215000129 161219216000129 161219217000129 161219218000129 170217101000129 170217102000129 170217103000129 170217104000129 170217105000129 170217106000129 170217107000129 170217108000129 170217109000129 170217110000129 170217111000129 170217112000129 170217113000129 170217114000129 170217115000129 170217116000129 170301201000129 170301202000129 170301203000129 170301204000129 170301205000129 170301206000129 170301207000129 170301208000129 170301209000129 170301210000129 170301211000129 170301212000129 170301213000129 170301214000129 170301215000129 170301216000129 170301217000129 170308105000129 170308106000129 170308109000129 170308110000129 170308115000129 170308116000129 170308118000129 170308119000129 170308121000129 170308201000129 170308203000129 170308204000129 170308205000129 170308206000129 170308207000129 170308208000129 170308209000129 170308210000129 170308212000129 170308214000129 170308215000129 170308216000129 170308217000129 170308218000129 170308220000129 170308221000129 170308222000129 170605101000129 170605102000129 170605103000129 170605104000129

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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