Ruckers Makin Batch Candies Recall: RUCKER S MAKIN BATCH CANDIES (RMBC) initiated a voluntary recall of The Toothsome Chocolate Emporium Dark Chocolate Coffee Beans, Dark Chocolate Cranberries, and Dark Chocolate Peanuts following supplier's recall due to undeclared allergen milk.

🇺🇸 United States

1. October 31, 2017 - Recall initiated
2. December 6, 2017 - Reported by source
3. March 29, 2018 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-0404-2018

Event ID

78433

Status

Terminated

Classification

Class II

Company

Ruckers Makin Batch Candies

Product description

The Toothsome Chocolate Emporium Dark Chocolate Cranberries. The affected product is packaged in 8 oz. clear bag within a gold Toothsome Chocolate Emporium box, 24/case

Quantity

912 units

Reason

RUCKER S MAKIN BATCH CANDIES (RMBC) initiated a voluntary recall of The Toothsome Chocolate Emporium Dark Chocolate Coffee Beans, Dark Chocolate Cranberries, and Dark Chocolate Peanuts following supplier's recall due to undeclared allergen milk.

Recall initiation date

October 31, 2017

Report date

December 6, 2017

Classification date

Not published in this source record

Termination date

March 29, 2018

Distribution pattern

Domestic Only: Florida

UPC, lot, and code information

UPC 400013041067, 400013041098 and 400013041098. This only affects packages with best by codes ranging from 05/11/17 thru 10/09/18

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 78433 with 2 other product entries in Public Health Trace.

Responsible company: Ruckers Makin Batch Candies

Other recalls from Ruckers Makin Batch Candies

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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