Recalls / Class II
Class IIF-1703-2016
Product
Bolthouse Farms Coffee Protein Plus: 30 g protein per bottle + 21 vitamins & minerals. Packaged in 11 oz./325 mL - item number PPJ3BF9; 15.2 oz/450 mL item number: PPJ4BF6; 32 oz./946 mL; item number PPJQBF6: Selling Unit UPC Case GTIN 11 oz. 0-71464-01869-6 1-00-71464-01869-3; 15.2 oz. 0-71464-01627-2 1-00-71464-01627-9; 32 oz 0-71464-01628-9 1-00-71464-01628-6; Bolthouse Juice Products, LLC, Bakersfield, CA 93307
- Type
- Food
- Affected lot / code info
- 11 oz; - Best By: 7/7/16 and 7/23/16 and 8/19/16; All Production Times; Lots: BV116D24A2PP090 BV116E21A2PP090 BV216D24A2PP090 BV316D08A2PP090; 15.2 oz - Best By : 6/23/16 and 7/20/16 and 7/21/16 and 8/11/16 and 8/22/16 and 9/10/16; All Production Times. Lots: BV216C25A2PP090 BV116D21A2PP090 BV116E13A2PP090 BV116E24A2PP090 BV216D21A2PP090 BV216E13A2PP090 BV216E24A2PP090 BV216F12A2PP090 BV316D21A2PP090 BV316D22A2PP090 BV316E13A2PP090 BV316F12A2PP090; 32 oz. US - Best By: 7/11/16 and 7/26/16 and 8/10/16 and 9/12/16, All Production Times; Lots: BV116D12A2PP090 BV116D27A2PP090 BV116F14A2PP090 BV216D27A2PP090 BV216E12A2PP090 BV316D12A2PP090 BV316E12A2PP090.
- Quantity
- 3,814,275 units; 624,148 cases - all varieties
Why it was recalled
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.
Recalling firm
- Firm
- Wm Bolthouse Farms Inc
- Notification channel
- Press Release
- Type
- Voluntary: Firm initiated
- Address
- 7200 E Brundage Ln, N/A, Bakersfield, California 93307-3016
Distribution
- 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
Timeline
- Recall initiated
- 2016-06-22
- FDA classified
- 2016-07-15
- Posted by FDA
- 2016-07-27
- Terminated
- 2017-11-06
- Status
- Terminated
Source: openFDA Food Enforcement endpoint. Recall record F-1703-2016. The FDA issues recall classifications as health-hazard assessments, not legal findings.