Clio Strawberry Granola & Yogurt Parfait Bar Net Wt. 1.94 OZ (55g ) UPC: 854021008152 Packaged in a cardboard box.
Summary
The FDA issued a Class I for Clio Strawberry Granola & Yogurt Parfait Bar Net Wt. 1.94 OZ (55g ) UPC: 8540210 by Clio LLC. Reason: Possible contamination with Listeria monocytogenes.
Details
Source
Food Recall
External ID
F-0697-2023
Action Date
2023-04-12
Status
Terminated
Category
food
Product Description
Clio Strawberry Granola & Yogurt Parfait Bar Net Wt. 1.94 OZ (55g ) UPC: 854021008152 Packaged in a cardboard box.
Lot/Code Info: 048C2023 Expiration date:4/30/2023
Quantity Affected: 581 cases of 10 single units
Reason for Recall
Possible contamination with Listeria monocytogenes
Distribution
Product distributed to distribution centers in IL, SC, MO, WA, GA, MN, FL, NC, ME, and CA. Then further distributed to retail stores in IA, IL, VA, WI, and NC.
Type: Voluntary: Firm initiated
Recall Initiated: 2023-03-07
Company
Piscataway, NJ
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
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 I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
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 (Clio LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Clio LLC have FDA actions?
This is the only FDA action we have on record for Clio LLC in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0697-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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