World Finer Foods, Inc. Recall: The front of the product label says no added salt, but sea salt is correctly listed in the ingredient statement on the back. - F-0524-2018

🇺🇸 United States

1. December 7, 2017 - Recall initiated
2. January 10, 2018 - Reported by source
3. June 19, 2019 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-0524-2018

Event ID

78717

Status

Terminated

Classification

Class II

Company

World Finer Foods, Inc.

Product description

Rapunzel Vegetable Bouillon ( no added salt ), 2.4 oz. net weight, in a thick paper sleeve containing 8 foil-wrapped bouillon cubes, 12 units per case .

Quantity

20,550 cases were distributed

Reason

The front of the product label says no added salt, but sea salt is correctly listed in the ingredient statement on the back.

Recall initiation date

December 7, 2017

Report date

January 10, 2018

Classification date

Not published in this source record

Termination date

June 19, 2019

Distribution pattern

Distribution was nationwide.

UPC, lot, and code information

Lot numbers 112075, 113390, 114805, 116205, 118230 and 119631.

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

E-Mail

Source last updated

Not tracked separately from the Public Health Trace retrieval date below

Public Health Trace retrieval date

July 18, 2026 ET

Responsible company: World Finer Foods, Inc.

Other recalls from World Finer Foods, Inc.

Where this information comes from

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

This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information. See FDA Enforcement Reports versus recall announcements for how that database differs from a press-release-style announcement.

New to reading a recall record? See how to read an FDA recall record and what recall statuses mean.

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?

FDA classifies this recall as Class II. See how to read an FDA recall record (linked above) for what each classification level means.

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 responsible agency's published instructions, linked below -- recall guidance is set by that agency, not by Public Health Trace.

Official guidance and record verification

Public Health Trace does not provide medical advice -- review the linked official source below for current, authoritative information.

How to interpret this historical record

This record is preserved as published by FDA, as of June 19, 2019.

Status as reported: Terminated.

This page does not imply a current danger or a current consumer instruction -- review the official source for the most current information.

View the official FDA source

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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