Shoreline Fruit, LLC Recall: Shoreline Fruit is voluntarily recalling select Shoreline Fruit bulk and Cherry Bay Orchards branded dark chocolate coated cherry products due to supplier's recall of undeclared allergen milk in dark chocolate.

🇺🇸 United States

1. October 31, 2017 - Recall initiated
2. November 29, 2017 - Reported by source
3. March 21, 2018 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-0336-2018

Event ID

78434

Status

Terminated

Classification

Class II

Company

Shoreline Fruit, LLC

Product description

Shoreline Fruit Dark Choc Covered Montmorency Cherries packaged in 25-pound corrugated box

Quantity

9182 cases

Reason

Shoreline Fruit is voluntarily recalling select Shoreline Fruit bulk and Cherry Bay Orchards branded dark chocolate coated cherry products due to supplier's recall of undeclared allergen milk in dark chocolate.

Recall initiation date

October 31, 2017

Report date

November 29, 2017

Classification date

Not published in this source record

Termination date

March 21, 2018

Distribution pattern

Domestic: AK AL AR AZ CA CO CT DC DE FL GA HI IA IL IN KS KY MA MD ME MI MN MO MS MT NC ND NE NH NJ NM NV NY OH OK OR PA SC SD TN TX UT VA VT WA WI WV Foreign: Canada, Vietnam VA/DOD: None

UPC, lot, and code information

UPC/Product Code Description Size CHDC025Z Shoreline Fruit Dark Choc Covered Montmorency Cherries 25 lb. UPC/Product Code Description Size 8 46659 00048 6 Dried Dark Chocolate Covered Cherries 6 oz. 8 46659 00039 4 Dried Dark Chocolate Covered Cherries 24 oz. Lot numbers: 25 lb CHDC25Z Lot Code 032017 032117 032217 032317 032916 052617 053117 060316 060716 060916 083017 092717 102016 102116 102416 112116 112316 12 ct 6oz CHDCP0606ZCBO Lot Code 040918 100717 CHDCP0612ZCBO Lot Code 010318 010418 011218 011718 012118 012218 021618 022318 022718 022818 031518 031918 033118 040418 041418 042418 042518 042618 050118 050318 050418 050518 050618 051018 051818 052418 060918 061918 062018 062118 062618 062718 062818 070117 070217 071318 072118 081517 081617 081618 081718 081818 091717 092117 092217 092317 100717 110217 110317 120717 120817 122117 122317 122617 CHDCP0612ZCBOE Lot Code 070217 081517 091717 100717 12 ct Total 6 ct 6oz CHDCP0606ZCBO Lot Code 011318 032218 042918 050118 050918 051018 062718 070118 071018 072118 081618 110217 122617 10 ct 24 oz CHDCP2410ZCBO Lot Code 092918 10 ct Total 8 ct 24 oz CHDCP2408ZCBO Lot Code 030718 040418 050518 050918 051018 051818 060918 080818 081317 081618 091717 100918 101018 102018 110217 122617 CHDCP2408ZCBOE Lot Code 091717

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

Press Release

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 78434 with 1 other product entry in Public Health Trace.

Responsible company: Shoreline Fruit, LLC

Other recalls from Shoreline Fruit, 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
Alaska	1
Alabama	1
Arkansas	1
Arizona	1
California	1
Colorado	1
Connecticut	1
District of Columbia	1
Delaware	1
Florida	1
Georgia	1
Hawaii	1
Iowa	1
Illinois	1
Indiana	1
Kansas	1
Kentucky	1
Massachusetts	1
Maryland	1
Maine	1
Michigan	1
Minnesota	1
Missouri	1
Mississippi	1
Montana	1
North Carolina	1
North Dakota	1
Nebraska	1
New Hampshire	1
New Jersey	1
New Mexico	1
Nevada	1
New York	1
Ohio	1
Oklahoma	1
Oregon	1
Pennsylvania	1
South Carolina	1
South Dakota	1
Tennessee	1
Texas	1
Utah	1
Virginia	1
Vermont	1
Washington	1
Wisconsin	1
West Virginia	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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