Beachbody Hardcore Base Shake recall
Recalled by Beachbody Llc · Santa Monica, CA, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
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.
A label that does not match the product can hide an ingredient someone must avoid, or show a wrong use-by date. All labeling errors recalls.
What was recalled
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.
Quantity: 4627
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
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
Where it was sold
Nationwide.
Puerto Rico
FDA's distribution note: Nationwide (U.S. and Puerto Rico) and internationally in the following countries; Virgin Islands, Canada, and Palau.
Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- Beachbody Llc
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Nov 12, 2014
- In FDA report of
- Dec 24, 2014
- Terminated
- Feb 12, 2015
- FDA recall number
- F-0742-2015 · event 69772
- Official record
- FDA enforcement report search