Turner's Peach Whole Milk Cottage Cheese 5.3oz. (150g) UPC:3573300167
Summary
The FDA issued a Class II for Turner's Peach Whole Milk Cottage Cheese 5.3oz. (150g) UPC:3573300167 by Titusville Dairy Products Co.. Reason: Bacterial spoilage in cottage cheese.
Details
Source
Food Recall
External ID
F-0040-2023
Action Date
2022-10-26
Status
Terminated
Category
food
Product Description
Turner's Peach Whole Milk Cottage Cheese 5.3oz. (150g) UPC:3573300167
Lot/Code Info: " 7/20/22 " 7/27/22 " 8/03/22 " 8/24/22 " 8/31/22 " 9/7/22 " 9/14/22
Quantity Affected: 3966 units
Reason for Recall
Bacterial spoilage in cottage cheese
Distribution
Distributed to the recalling firm's direct consignee in PA.
Type: Voluntary: Firm initiated
Recall Initiated: 2022-09-16
Company
Titusville, PA
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 41 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Titusville Dairy Products Co. has 4 FDA actions in our database, including 4 recalls.
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 (Titusville Dairy Products Co.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Titusville Dairy Products Co. have FDA actions?
Titusville Dairy Products Co. has 4 FDA actions in our database, including 4 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0040-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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