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FDA source record Class II Terminated

BODYARMOR SportWater 24/700mL; BODYARMOR SportWater 12/1Liter; BODYARMOR SportWater 24/20oz 6PK; BODYARMOR SportWater 2x6/1 Liter; BODYARMOR SportWater 15/700mL Club; BODYARMOR ...

Recall Date: 2023-02-28 Recalling Firm: BA Sports Nutrition, LLC Record Ref: F-0646-2023

FINDARECALL QUICK READ

What this record tells you

This FDA record concerns BODYARMOR SportWater 24/700mL; BODYARMOR SportWater 12/1Liter; BODYARMOR SportWater 24/20oz 6PK; BODYARMOR SportWater 2x6/1 Liter; BODYARMOR SportWater 15/700mL Club; BODYARMOR ... and names BA Sports Nutrition, LLC as the recalling firm. Use the source fields below to narrow the match, then verify the exact item and current remedy on the issuing-agency page.

  • Firm: BA Sports Nutrition, LLC
  • Classification: Class II
  • Status: Terminated
  • Recall date: 2023-02-28
Best identifiers to check for a FDA record

Compare UPC/GTIN, lot or batch code, package size, flavor or variety, and any best-by/use-by date listed in the notice.

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Product Description & Identification

BODYARMOR SportWater 24/700mL; BODYARMOR SportWater 12/1Liter; BODYARMOR SportWater 24/20oz 6PK; BODYARMOR SportWater 2x6/1 Liter; BODYARMOR SportWater 15/700mL Club; BODYARMOR SportWater 15/1L Club

Reason for Recall / Hazard Identified

Potential for plastic pieces in product

How to Check Whether Your Product Matches

A matching product name or photograph is not enough by itself. Compare every identifier available on your item or packaging with the official notice.

  1. Confirm the full product and brand or recalling-firm name.
  2. Compare package size, color, flavor, model, style, or configuration when listed.
  3. Check UPC, lot, batch, serial, date code, recall number, or USDA establishment number.
  4. Review the recall date and distribution information without assuming every seller is listed.
  5. Open the official FDA source below and follow its current instructions.

If a required identifier is missing, contact the recalling company or issuing agency through the official notice rather than guessing.

Consumer Action Recorded in the Source

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Distribution & Affected States

IL, KS, SD, OR, WA, MN, UT, AL, IA, TX, AR

Verify With the Issuing Agency

This record was last updated in our index on 2026-08-09 21:59:13 UTC. Because recall enforcement statuses and instructions evolve, always verify details directly with the issuing government agency.

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Record Transparency

Issuing agency
FDA
Source ID
F-0646-2023
Indexed update
2026-08-09 21:59:13 UTC
Official source
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