Class IITerminated · reported 2014-12-24

Beachbody Hardcore Base Shake Lot #42932B22, #42931A22, and #42902B22 Black HDPE…

Beachbody Llc recalled this product and the FDA reported the enforcement action on 24 December 2014 as Class II. The recall was initiated by the firm. During an investigation of label issuance and reconciliation at the firm's contract manufacturer it was discovered that 948 labels of Beachbody Extreme Nutrition Base Shake entered into Beachbody Extreme Nutrition Fuel Shot production. Therefore some bottles of Beachbody Extreme Nutrition Fuel Shot were labeled Beachbody Extreme Nutrition Base Shake.

The record

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Product: Beachbody Hardcore Base Shake Lot #42932B22, #42931A22, and #42902B22 Black HDPE container with Black Lid. Label stated weight of 1 lb. 12.2 oz. (800 g.) Lot code information located on the bottom of the container in yellow ink.
Reason for recall: During an investigation of label issuance and reconciliation at the firm's contract manufacturer it was discovered that 948 labels of Beachbody Extreme Nutrition Base Shake entered into Beachbody Extreme Nutrition Fuel Shot production. Therefore some bottles of Beachbody Extreme Nutrition Fuel Shot were labeled Beachbody Extreme Nutrition Base Shake.
Recalling firm: Beachbody Llc
Firm location: Santa Monica, California, United States
Classification: Class II
Status: Terminated
Recall number: F-0742-2015
Quantity: 4627
Distribution: Nationwide (U.S. and Puerto Rico) and internationally in the following countries; Virgin Islands, Canada, and Palau.
Initiated: 12 November 2014
Reported by FDA: 24 December 2014
Terminated: 12 February 2015
Firm notified by: E-Mail
Product codes: Lot code information located on the bottom of the container in yellow ink. Lots Involved: 1. LOT # 42932B22 EXP. 10/16 2. LOT# 42931A22 EXP. 10/16 3. LOT# 42902B22 EXP. 10/16

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 record is the only one the FDA opened for its recall event, so it covers a single product code.
The recall ran for 3 months, from 12 November 2014 to termination on 12 February 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 6 weeks after the firm began the recall.
The product description on this record names no food this site can classify, so it appears on no food-type page. That is a limit of the description rather than of the recall.

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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.