Class IITerminated · reported 2014-12-24

Odwalla Chocolate Protein Shake, 15.2 fl. oz, and 32 fl. oz bottles, Distributed by…

Coca-Cola Company (The) recalled this product and the FDA reported the enforcement action on 24 December 2014 as Class II. The recall was initiated by the firm. There is the potential that some of the bottles could exhibit spoilage before end of shelf life.

The record

Every field below is published by the FDA in the openFDA food enforcement database. Check the FDA notice before acting on any recall: this page is a reading of the public record, not a substitute for it.

Product
Odwalla Chocolate Protein Shake, 15.2 fl. oz, and 32 fl. oz bottles, Distributed by: Odwalla, Inc., Dinuba, CA 93618.
Reason for recall
There is the potential that some of the bottles could exhibit spoilage before end of shelf life.
Firm location
Atlanta, Georgia, United States
Classification
Class II
Status
Terminated
Recall number
F-0711-2015
Quantity
30,390 units (32oz) and 158,880 units (15.2oz) total
Distribution
U.S. Nationwide
Initiated
23 October 2014
Reported by FDA
24 December 2014
Terminated
13 January 2015
Firm notified by
Visit
Product codes
UPC: 014054 13505 2, Production Date: 09/19/14 and 09/20/14, Best By Date: DEC 18 14 and DEC 19 14 (15.2oz) and UPC: 0 14054 13504 5, Production Date: 09/13/214 and 09/14/14, Best By Date: DEC 12 14 and DEC 13 14 (32.0 oz)

Reading this record

Five things about this record are not in the record itself, and each one changes how it should be read.

  • Class II means the FDA judged a remote probability of serious harm, or a probability of temporary or medically reversible harm. The class is assigned by an agency health hazard evaluation under 21 CFR 7.41, not by the firm.
  • The firm started this recall itself. Most FDA food recalls are voluntary, and a recall is a food safety plan working rather than failing. The circumstances in which the agency asks for one instead are set out in 21 CFR 7.45.
  • This is one of 2 records covering the same recall event. The FDA opens one enforcement record per product code, so a recall of a product line appears here many times. Counting these records as 2 separate recalls, which almost every published figure does, overstates it by a factor of 2. All 2 of them are listed on this page.
  • The recall ran for 3 months, from 23 October 2014 to termination on 13 January 2015. Termination means the agency judged that all reasonable effort had been made, under 21 CFR 7.55, and it says nothing about whether product remained in circulation.
  • The FDA published the enforcement report 2 months after the firm began the recall.
  • Recalls of a snack or confectionery product run a median of 7 months, so this one was shorter than usual for its category. Snacks and confectionery recall for allergens more than for anything else, because a chocolate or a coated snack passes through shared equipment carrying milk, soy and nuts, and the label is the only control between them and the consumer.

What this recall was for

Spoilage and mould

A spoilage recall means the food degraded before its date: mould growth, unintended fermentation, swelling or rancidity, usually traced to a seal, a formulation or a storage temperature.

A preventive controls plan covers spoilage under the clauses below. This is where the control belongs, not a finding against any firm named on this page: a recall record states a reason, and most of these recalls were initiated by the firm itself.

21 CFR 117.93
Warehousing and distribution: storage and transport under conditions that protect food against contamination and against deterioration of the food and its container.
21 CFR 117.80(b)(3)
Time and temperature: holding food at temperatures that do not allow microorganisms to grow, and for no longer than the process allows.

Filed under snacks and confectionery. A product can sit in more than one.

Every product in this recall

The FDA opened 2 enforcement records for this one recall, one per product code. This page carries all of them; the 1 below each have their own page with that product’s lot codes and distribution, and search engines are pointed here for the recall as a whole.

The other 1 records of FDA event 69801
ReportedProductFirmReasonClass
2014-12-24Odwalla Vanilla Almondo Protein, 15.2 fl. oz bottles, Distributed by: Odwalla, Inc., Dinuba, CA 93618.Coca-Cola Company (The)There is the potential that some of the bottles could exhibit spoilage before end of shelf life.Class II

Other snacks and confectionery recalls for the same reason

These are the closest records in the corpus: the same kind of food, recalled for a hazard this record also names. Unlike the firm’s own records below, they come from different companies, which is what makes them a pattern rather than a history.

ReportedProductFirmReasonClass
2025-09-03Hostess Ding Dongs CHOCOLATE CAKE WITH CREAMY FILLING 2.55 oz twin pack UPC 8 88109 01002 7; 10-1.28 oz carton (12.7 oz) UPC 8 88109 11061 1; 16-1.28 oz carton (20.31 oz) Individual selling unit - UPC 8 88109 01182 6 16-count selling unit - UPC 8 88109 11092 5The J.M. Smucker CompanyMold. The firm noticed an increase in customer complaints. They conducted a root cause investigation and discovered that one of their coolers had malfunctioning.Class II
2025-06-11Sysco Classic chocolate pudding, 7lb #10 metal can, UPC 074865103817, 6 cans per case. Bay Valley Foods Thank You chocolate pudding, 7lb #10 metal can, UPC 041820062205 , 6 cans per case.Treehouse FoodsPost process damage to containers, potential for microbial growth, swollen and or exploding containersClass II
2025-04-23LEGALLY ADDICTIVE THE O.G. COOKIES MADE FROM CRACKERS+TOFFEE+CHOCOLATE+SEA SALT NET WT. 4.7OZ (133G) UPC 8 54766 00802 8 & 1.34OZ (38G) UPC 8 54766 02800 4Legally Addictive FoodsThe firm received complaints of a "rancid taste" from consumers.Class II
2024-10-02Montreal Fudge brand Chocolate Fudge with Nuts; 5.6ozAUTHENTIK FUDGEProduct may be contaminated with mold.Class II
2024-08-21Fox's u-bet Sugar-Free Chocolate Flavored Syrup, 18oz, UPC 070216246004, 12 retail units per wholesale caseSUBCO FOODS INCCustomer complaint for bloated bottles. Testing and examination of these lots has revealed they did not meet specifications, including elevated pH and water activity levels. This may be indicative of microbiological activity, and concurrent risk of food-borne illness.Class III
2023-10-04Cerebelly Smart Bar; Apple Kale flavor; 5 pk and 7 pk; ambient storageCEREBELLY INCSurface mold visible on productClass II
2023-10-04Cerebelly Smart Bar; Strawberry Beet flavor; 5 pk and 7 pk; ambient storageCEREBELLY INCSurface mold visible on productClass II
2023-10-04Cerebelly Smart Bar; Blueberry Banana flavor; 5 pk; ambient storageCEREBELLY INCSurface mold visible on productClass II

Other records from Coca-Cola Company (The)

The FDA opens one enforcement record per product code, so several of these are frequently one recall event. 13 other records name this firm.

ReportedProductFirmReasonClass
2016-10-12Diet Dr Pepper, 12 oz. can/24 pack, UPC 078000083132; Diet Dr Pepper, 12 oz. can/6 pack, UPC N/A; Diet Dr Pepper, 12 oz. can/20 pack, UPC 078000083095; Dr Pepper, 12 oz. can/6 pack, UPC N/A; Dr Pepper , 12 oz. can/ 20 pack, UPC 078000082098; Dr Pepper 12 oz. can/ 12 pack, UPC 078000082166; Dr Pepper, 12 oz. can/24 pack, UPC 078000082135Coca-Cola Company (The)In a small percentage of the cans, when opened, the oval covering for the hole, which normally is pushed down into the can, instead opens upward. This produces a loud "pop" sound. Recall initiated on 4/29/16.Class II
2016-10-12Coca-Cola, 16 fl. oz. can/12 pack, UPC 049000054318; Coca-Cola, 12 oz. can/12 pack, UPC 049000028904; Coca-Cola Zero, 12 oz. can/12 pack, UPC 049000042559; Diet Coke, 12 oz. can/24 pack, UPC 049000010633; Diet Coke, 12 oz. can/12 pack, UPC 049000028911; Cherry Coke, 12 oz. can/12 pack, UPC 049000031034Coca-Cola Company (The)In a small percentage of the cans, when opened, the oval covering for the hole, which normally is pushed down into the can, instead opens upward. This produces a loud "pop" sound. Recall initiated on 4/29/16.Class II
2016-10-12Sprite Zero, 12 oz. can/12 pack, UPC 049000037111; Sprite, 12 oz. can/6 pack, UPC N/A; Sprite, 12 oz. can/12 pack, UPC 049000028928; Sprite, 12 oz. can/20 pack, UPC 049000014655Coca-Cola Company (The)In a small percentage of the cans, when opened, the oval covering for the hole, which normally is pushed down into the can, instead opens upward. This produces a loud "pop" sound. Recall initiated on 4/29/16.Class II
2016-09-28Huberts Lemonade Blackberry, 16 Fl. Oz. (473 ml), Manufactured for: Hamsen Beverage, Tustin, CA 92780.Coca-Cola Company (The)The product may contain foreign material (glass) in some bottles.Class II
2016-09-28Huberts Original Lemonade, 16 Fl. Oz. (473 ml), Manufactured for: Hamsen Beverage, Tustin, CA 92780.Coca-Cola Company (The)The product may contain foreign material (glass) in some bottles.Class II
2016-09-28Huberts Lemonade Strawberry, 16 Fl. Oz. (473 ml), Manufactured for: Hamsen Beverage, Tustin, CA 92780.Coca-Cola Company (The)The product may contain foreign material (glass) in some bottles.Class II
2016-09-28Huberts Lemonade Watermelon, 16 Fl. Oz. (473 ml), Manufactured for: Hamsen Beverage, Tustin, CA 92780.Coca-Cola Company (The)The product may contain foreign material (glass) in some bottles.Class II
2016-06-15Honest Kids-Super Fruit Punch, Organic Juice Drink, 59 fluid oz. bottle, 006 57622 41273 7, Honest Tea, Inc., 4827 Bethesda Ave., Bethesda, MD 20814.Coca-Cola Company (The)The label does not list apple juice ingredient present in the beverage.Class II
2016-03-23Citrus Flavored Soda Mello Yello, 12 fl. oz. (355 ml), Canned under authority of The Coca-Cola Company, Atlanta, GA 30313, UPC 497250Coca-Cola Company (The)Undeclared aspartame in the product.Class II
2015-07-01Diet Dr. Pepper, 8 x 12 fl. oz. PET bottle, Bottled under the authority of Dr. Pepper Company, 5301 Legacy Drive, Plano, TX 85024.Coca-Cola Company (The)A Diet Dr. Pepper labeled product contain regular Dr. Pepper.Class II

All 14 records for Coca-Cola Company (The)

All 2014 recalls · All FDA food recall data

21 CFR 117.93 is the clause behind this recall, and it is one somebody has to produce evidence for at their next audit. Krolda maps supplier documents to the clause they satisfy in FSSC 22000, IFS Food and 21 CFR 117, and routes the corrective action when the evidence is missing.

Early access

Recall records come from the openFDA food enforcement API, published by the U.S. Food and Drug Administration in the public domain. Krolda adds the hazard classification and the clause mapping; neither is an FDA determination. Always check the FDA notice before acting on a recall.