Hardcore Base Shake (Beachbody) – Label reconciliation issue (2014)
Class II: A situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Class II recall indicates potential for temporary health effects.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
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.
Brand
Beachbody Llc
Lot Codes / Batch Numbers
Not specified in FDA notice. Check official source for details.
Products Sold
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
Beachbody Llc is recalling Beachbody Hardcore Base Shake Lot #42932B22, #42931A22, and #42902B22 Black HDPE container with Bl due to During an investigation of label issuance and reconciliation at the firm's contract manufacturer it was discovered that 948 labels of Beachbody Extrem. This is a Class I recall, indicating a high risk of serious health consequences. Based on FDA enforcement report.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
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.
Recommended Action
Per FDA guidance
Consumers should stop using the product and contact the recalling firm or return it to the place of purchase.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 6, 2026