Bulletproof 360 Inc Recall: Fudge Brownie Collagen Protein Bite is recalled because it has the potential to be contaminated with Listeria monocytogenes.

🇺🇸 United States

1. June 14, 2017 - Recall initiated
2. July 12, 2017 - Reported by source
3. November 8, 2017 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-2437-2017

Event ID

77548

Status

Terminated

Classification

Class I

Company

Bulletproof 360 Inc

Product description

Fudge Brownie Collagen Protein Bite. Each Bite is packed in foil wrapper, net wt. per Bite 0.74 oz (21g). There 15 pieces packed in a box and the net wt. is 11.10 oz (315 g). Individual Bar UPC 815709021528. Box UPC 815709021535.

Quantity

1,321 boxes (or 22,055 bites)

Reason

Fudge Brownie Collagen Protein Bite is recalled because it has the potential to be contaminated with Listeria monocytogenes.

Recall initiation date

June 14, 2017

Report date

July 12, 2017

Classification date

Not published in this source record

Termination date

November 8, 2017

Distribution pattern

nationwide including Puerto Rico, U.S. Virgin Islands, and sold online at bulletproof.com. Products were distributed internationally in the following countries: Australia, Bahrain, Bermuda, Bolivia, Brazil, Brunei Darussalam, Canada, Cayman Islands, China, Finland, France, Germany, Guam, Hong Kong, Hungary, Iceland, Israel, Japan, Korea, Kuwait, Liechtenstein, Macau, Malaysia, Malta, Mexico, Monaco, Netherlands, New Zealand, Norway, Oman, Philippines, Romania, Saudi Arabia, Singapore, Spai

UPC, lot, and code information

UPC 815709021528; Lot # 1517-01, Use by Date 12/27/2017; Lot # 1227-01, Use by Date 11/28/2017; Lot # 1327-01, Use by Date 12/8/2017.

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 77548 with 4 other product entries in Public Health Trace.

Responsible company: Bulletproof 360 Inc

Other recalls from Bulletproof 360 Inc

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 I mean?

A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.

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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