THE CHAI BOX CHAI CONCENTRATE UNSWEETENED 16FL OZ/473ML glass bottles UPC 7 93611 81925 2 REGRIGERATE AFTER OPENING. USE
Summary
The FDA issued a Class III for THE CHAI BOX CHAI CONCENTRATE UNSWEETENED 16FL OZ/473ML glass bottles UPC 7 9361 by The Chai Box. Reason: Potential to be contaminated with Clostridium botulinum. Product was tested and found to have pH level of 4.9..
Details
Source
Food Recall
External ID
F-0079-2023
Action Date
2022-11-02
Status
Terminated
Category
food
Product Description
THE CHAI BOX CHAI CONCENTRATE UNSWEETENED 16FL OZ/473ML glass bottles UPC 7 93611 81925 2 REGRIGERATE AFTER OPENING. USE WITHIN 14 DAYS and 64FL OZ/1892ML plastic bottles KEEP REFRIGERATED USE WITHIN 7 DAYS OF OPENING UPC 7 93611 81926 9. INGREDIENTS Water, Black Teas, Spices - Cardamom, Cinnamon, Fennel, Cloves, Ginger ATLANTA, GA THECHAIBOX.COM
Lot/Code Info: BEST BY dates between 9/22/2022 and 03/16/2023
Quantity Affected: 1341 16oz bottles & 268 64oz bottles
Reason for Recall
Potential to be contaminated with Clostridium botulinum. Product was tested and found to have pH level of 4.9.
Distribution
Product was shipped to the following states: AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI & WY.
Type: Voluntary: Firm initiated
Recall Initiated: 2022-09-23
Company
Marietta, GA
Context & Analysis
This is a Class III recall. Class III recalls involve products unlikely to cause adverse health consequences, but that violate FDA regulations.
This was one of 42 food recalls issued in the same week, part of 204 food-related FDA actions this month.
The Chai Box has 2 FDA actions in our database, including 2 recalls.
Frequently Asked Questions
What is a Class III recall?
A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.
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 (The Chai Box) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does The Chai Box have FDA actions?
The Chai Box has 2 FDA actions in our database, including 2 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0079-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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