FDA recall record

Lucky Spoon Bakery 7.25 oz recall — FDA F-0019-2021

Products are labeled gluten-free. A batch of flour from the raw material supplier tested positive for gluten so the firm immediately initiated a recall of…

Class IIclassification
F-0019-2021official record ID
Oct 21, 2020report date

Recall record at a glance

Official recordF-0019-2021
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmLucky Spoon Bakery, LLC
Report dateOct 21, 2020
Recall initiation dateAug 26, 2020
Quantity118 cases of 12
LocationSalt Lake City, UT, United States

Official product description

Lucky Spoon Bakery Gluten Free Utterly Almond Muffins, 7.25 oz. plastic clam shell containing 6 muffins, UPC 8-50489-00305-0, P.O. Box 2954, Salt Lake City, UT 84110. 12 packages/case

Why the product was recalled

Products are labeled gluten-free. A batch of flour from the raw material supplier tested positive for gluten so the firm immediately initiated a recall of the affected products.

Distribution information

CA, CO, CT, FL, GA, TX, UT, WI. Nationwide through drop ship.

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: 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.

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