Purity Sweet Acidophilus 1% Lowfat Milk packaged in paper half pint cartons - 50 cartons per case, Keep Refrigerated
Summary
The FDA issued a Class II for Purity Sweet Acidophilus 1% Lowfat Milk packaged in paper half pint cartons - 50 by DFA Dairy Brands Fluid, LLC. Reason: 1% Low Fat Milk potentially contaminated with sanitizer.
Details
Source
Food Recall
External ID
F-0694-2023
Action Date
2023-04-12
Status
Terminated
Category
food
Product Description
Purity Sweet Acidophilus 1% Lowfat Milk packaged in paper half pint cartons - 50 cartons per case, Keep Refrigerated
Lot/Code Info: Batch No: Mar 24 UPC: 04190007778 Manufacturer No: Grad A IMS # 47-118 Best By Mar 24 Time Stamp 0930 to 0933
Quantity Affected: 547 cartons
Reason for Recall
1% Low Fat Milk potentially contaminated with sanitizer
Distribution
Alabama
Type: Voluntary: Firm initiated
Recall Initiated: 2023-03-10
Company
Nashville, TN
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 47 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 (DFA Dairy Brands Fluid, LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does DFA Dairy Brands Fluid, LLC have FDA actions?
This is the only FDA action we have on record for DFA Dairy Brands Fluid, LLC in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0694-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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