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.
Class I - DangerousWhat Should You Do?
- Check if you have this product: 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
- Do not eat it: Even if it looks and smells fine, do not consume this product.
- Throw it away or return it: You can return the product to the store for a full refund.
- Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
- Report problems: Report any issues to the FDA's Safety Reporting Portal.
⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.
Recall Details
- Company:
- Beachbody Llc
- 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.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- terminated
Product Information
Full Description:
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.
Product Codes/Lot Numbers:
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
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: F-0742-2015
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