BODYARMOR SportWater 24/700mL; BODYARMOR SportWater 12/1Liter; BODYARMOR SportWater 24/20oz 6PK; BODYARMOR SportWater 2x
Summary
The FDA issued a Class II for BODYARMOR SportWater 24/700mL; BODYARMOR SportWater 12/1Liter; BODYARMOR SportWa by BA Sports Nutrition, LLC. Reason: Potential for plastic pieces in product.
Details
Source
Food Recall
External ID
F-0646-2023
Action Date
2023-03-29
Status
Terminated
Category
food
Product Description
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
Lot/Code Info: All codes up to and including BB 021624 UNX LO4
Quantity Affected: approximately 21,000,000 bottles
Reason for Recall
Potential for plastic pieces in product
Distribution
IL, KS, SD, OR, WA, MN, UT, AL, IA, TX, AR
Type: Voluntary: Firm initiated
Recall Initiated: 2023-02-28
Company
Whitestone, NY
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 503 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (BA Sports Nutrition, LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does BA Sports Nutrition, LLC have FDA actions?
This is the only FDA action we have on record for BA Sports Nutrition, LLC in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0646-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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