FDA recall record

Refresco Beverages US a.) Great Value 8oz Apple Juice in 6pack recall — FDA F-1795-2024

Products contains inorganic arsenic above action level set in guidance to industry.

Class IIclassification
F-1795-2024official record ID
Sep 11, 2024report date

Recall record at a glance

Official recordF-1795-2024
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmRefresco Beverages US Inc.
Report dateSep 11, 2024
Recall initiation dateAug 26, 2024
QuantityTotal Products (all brands): 141,298 cases
LocationTampa, FL, United States

Official product description

a.) Great Value 8oz Apple Juice in 6pack; PET plastic bottle b.) Great Value 96oz Apple Juice; PET plastic bottle c.) Market Basket 100% apple juice; 64 oz; PET plastic bottle d.) Nice! 100% apple juice ; 64 oz; PET plastic bottle e.) Weis 100% apple juice; 64 oz; PET plastic bottle f.) Urban Meadow 100% apple juice; 64 oz; PET plastic bottle g.) Natures Nectar 100% apple juice; 64 oz; PET plastic bottle h.) Wellsley Farms 100% apple juice; 96 oz; PET plastic bottle i.) Solevita 100% apple juice; 64 oz; PET plastic bottle j.) Clover Valley 100% apple juice; 64 oz; PET plastic bottle k.) Tropical Delight 100% apple juice; 64 oz; PET plastic bottle

Why the product was recalled

Products contains inorganic arsenic above action level set in guidance to industry.

Distribution information

Great Value (8oz):IN, OH, PA, ME, NY, FL, AL, GA, VA, KY, SC Great Value (96 oz): PR, IN, PA, OH, VA, ME, NY, VA Market Basket 100% apple juice: ME Nice! 100% apple juice: GA, OH, PA, WI, FL Weis 100% apple juice: PA, MD Urban Meadow 100% apple juice: PA Natures Nectar 100% apple juice: NY, WI, OH, PA, IN, FL, GA, SC Wellsley Farms 100% apple juice: FL, NJ, MA Solevita 100% apple juice: VA Clover Valley 100% apple juice: SC, GA, OH, KY, FL, IN, NY Tropical Delight: NY

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Telephone.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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