FAIRLIFE MILK 8OZ / 6PK CHOCOLATE (multi-pack format of small single serve bottle); Date Code "MAY2722 FA"; Case UPC 008
Summary
The FDA issued a Class II for FAIRLIFE MILK 8OZ / 6PK CHOCOLATE (multi-pack format of small single serve bottl by Fairlife Llc. Reason: Product has potential for spoilage and lack of commercial sterility..
Details
Source
Food Recall
External ID
F-0012-2022
Action Date
2021-10-20
Status
Terminated
Category
food
Product Description
FAIRLIFE MILK 8OZ / 6PK CHOCOLATE (multi-pack format of small single serve bottle); Date Code "MAY2722 FA"; Case UPC 008-11620-02207-1; Unit UPC 008-11620-02206-4
Lot/Code Info: Date Code "MAY2722 FA"
Quantity Affected: 1,137 cases (each case contains 4 units of 6 bottles)
Reason for Recall
Product has potential for spoilage and lack of commercial sterility.
Distribution
Product was distributed to 8 retailers (in AZ, CA, OR, UT and WA) and 1 distributor (military)
Type: Voluntary: Firm initiated
Recall Initiated: 2021-09-24
Company
Chicago, IL
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 17 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 (Fairlife Llc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Fairlife Llc have FDA actions?
This is the only FDA action we have on record for Fairlife Llc in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0012-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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