Bounce Life Style HQ Recall: Cashew Cinnamon - Caf¿ Bounce is recalled because it has the potential to be contaminated with Listeria monocytogenes. This product contains sunflower kernels that were recalled by supplier SunOpta. - F-2403-2016

🇺🇸 United States

1. June 8, 2016 - Recall initiated
2. October 5, 2016 - Reported by source
3. November 3, 2016 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-2403-2016

Event ID

74430

Status

Terminated

Classification

Class I

Company

Bounce Life Style HQ

Product description

Australia -Cashew Cinnamon - Caf¿ Bounce, each bulk bag contains 60 pieces, and has UPC 29335805000494

Quantity

4428 bags

Reason

Cashew Cinnamon - Caf¿ Bounce is recalled because it has the potential to be contaminated with Listeria monocytogenes. This product contains sunflower kernels that were recalled by supplier SunOpta.

Recall initiation date

June 8, 2016

Report date

October 5, 2016

Classification date

Not published in this source record

Termination date

November 3, 2016

Distribution pattern

distributed nationwide in the US and in Australia, Canada, and United Kingdom.

UPC, lot, and code information

UPC 29335805000494; B.B. 09DEC16 F5 0406 B.B. 05MAR17 F6 1266

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

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 74430 with 2 other product entries in Public Health Trace.

Responsible company: Bounce Life Style HQ

Other recalls from Bounce Life Style HQ

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 I mean?

FDA classifies this recall as Class I. 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 November 3, 2016.

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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