Wm Bolthouse Farms Inc Recall: Bolthouse Farms is recalling 8 varieties of Protein Plus and Perfectly Protein drinks due to spoilage that may cause beverage to appear lumpy and have an unpleasant taste and odor. - F-1705-2016

🇺🇸 United States

1. June 22, 2016 - Recall initiated
2. July 27, 2016 - Reported by source
3. November 6, 2017 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-1705-2016

Status

Terminated

Classification

Class II

Company

Wm Bolthouse Farms Inc

Product description

Bolthouse Farms Strawberry Protein Plus: 30 g protein per bottle + 21 vitamins & minerals. Packaged in 15.2 oz/450 mL item number: PPCN4BF6; 32 oz/946 mL. - item number PPSWQBF6 Selling Unit UPC Case GTIN 15.2 oz. 0-71464-01890-0 1-00-71464-01890-7; 32 oz. 0-71464-01891-7 1-00-71464-01891-4; Bolthouse Juice Products, LLC, Bakersfield, CA 93307

Quantity

Not published in this source record

Reason

Bolthouse Farms is recalling 8 varieties of Protein Plus and Perfectly Protein drinks due to spoilage that may cause beverage to appear lumpy and have an unpleasant taste and odor.

Recall initiation date

June 22, 2016

Report date

July 27, 2016

Classification date

Not published in this source record

Termination date

November 6, 2017

Distribution pattern

Nationwide,and Canada, Jamaica Puerto Rico Tahiti Anguilla Antigua Aruba Barbados St. Maarten St. Thomas Qatar Lebanon UAE Bahrain Oman Kuwait Saudi Arabia Cayman Islands Guam Hong Kong American Samoa

UPC, lot, and code information

Not published in this source record

Voluntary or mandated

Not published in this source record

Initial notification method

Not published in this source record

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: Wm Bolthouse Farms Inc

Other recalls from Wm Bolthouse Farms 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 November 6, 2017.

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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