Plant Based Yogurt Culina Peach Cashew Nt Wt 5 oz. (142 g) UPC854724007254 packaged in glass container 12 jars per case
Summary
The FDA issued a Class II for Plant Based Yogurt Culina Peach Cashew Nt Wt 5 oz. (142 g) UPC854724007254 pack by EAT REAL FOOD LLC. Reason: Potential for glass to be found in product.
Details
Source
Food Recall
External ID
F-1409-2022
Action Date
2022-07-13
Status
Terminated
Category
food
Product Description
Plant Based Yogurt Culina Peach Cashew Nt Wt 5 oz. (142 g) UPC854724007254 packaged in glass container 12 jars per case
Lot/Code Info: Lot code - 06122CBCUCYPCB0725; Best by 10/31/2022
Quantity Affected: 13,725 cases total
Reason for Recall
Potential for glass to be found in product
Distribution
Nationwide to all states
Type: Voluntary: Firm initiated
Recall Initiated: 2022-06-15
Company
Austin, TX
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 53 food recalls issued in the same week, part of 204 food-related FDA actions this month.
EAT REAL FOOD LLC has 6 FDA actions in our database, including 6 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 (EAT REAL FOOD LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does EAT REAL FOOD LLC have FDA actions?
EAT REAL FOOD LLC has 6 FDA actions in our database, including 6 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1409-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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