Pariva Marinated Labneh Bites Za'atar; NET WT 8 OZ (225g); INGREDIENTS: YOGURT (CULTURED PASTEURIZED GRADE A MILK & CREA
Summary
The FDA issued a Class II for Pariva Marinated Labneh Bites Za'atar; NET WT 8 OZ (225g); INGREDIENTS: YOGURT ( by Pariva LLC. Reason: Product may be contaminated with mold..
Details
Source
Food Recall
External ID
F-1729-2024
Action Date
2024-08-21
Status
Terminated
Category
food
Product Description
Pariva Marinated Labneh Bites Za'atar; NET WT 8 OZ (225g); INGREDIENTS: YOGURT (CULTURED PASTEURIZED GRADE A MILK & CREAM, SKIM MILK, WHEY PROTEIN CONCENTRATE, SALT AND PECTIN), *SUNFLOWER OIL, *EXTRA VIRGIN OLIVE OIL, SESAME SEEDS, SPICES; CONTAINS: MILK, SESAME; Distributed by, Mayur, LLC, 196 Quincy St., Dorchester, MA 02121; KEEP REFRIGERATED; UPC 647297431201; Packaged in glass jars with metal or plastic lids
Lot/Code Info: Best By Dates: 10/21/24, 10/22/24, 12/5/24
Quantity Affected: 4261 units total for all products
Reason for Recall
Product may be contaminated with mold.
Distribution
MA, ME, NH, RI, NY, NJ, CT
Type: Voluntary: Firm initiated
Recall Initiated: 2024-07-15
Company
Dorchester, MA
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 125 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Pariva LLC has 3 FDA actions in our database, including 3 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 (Pariva LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Pariva LLC have FDA actions?
Pariva LLC has 3 FDA actions in our database, including 3 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1729-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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