FDA recall record

Pressery The label reads, "Golden Sunrise Cold Pressured Juice Carrot recall — FDA F-1095-2024

Bottle of juice was found at the store level with the incorrect sku label.

Class IIIclassification
F-1095-2024official record ID
Apr 3, 2024report date

Recall record at a glance

Official recordF-1095-2024
CategoryFood Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmPressery, LLC
Report dateApr 3, 2024
Recall initiation dateFeb 16, 2024
Quantity57 cases: 12 bottles per case: 684 bottles
LocationDenver, CO, United States

Official product description

The label reads, "Golden Sunrise Cold Pressured Juice Carrot, Orange, Pineapple, Lemon, Ginger & Turmeric 11 fl. oz."

Why the product was recalled

Bottle of juice was found at the store level with the incorrect sku label.

Distribution information

Distributed to retail stores throughout the U.S.

How to read the classification

FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.

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

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.