FDA recall record

WANABANA USA Schnucks APPLE SAUCE FRUIT POUCH, CINNAMON Net Weight: 3.2 oz recall — FDA F-0404-2024

North Carolina Department of Health and Human Services (NCDHHS) sampled product and found it to contain high levels of lead.

Class Iclassification
F-0404-2024official record ID
Nov 15, 2023report date

Recall record at a glance

Official recordF-0404-2024
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmWANABANA USA LLC
Report dateNov 15, 2023
Recall initiation dateOct 29, 2023
Quantity2,998,088 units (total)
LocationJacksonville, FL, United States

Official product description

Schnucks APPLE SAUCE FRUIT POUCH, CINNAMON Net Weight: 3.2 oz (90g) Pouches, 20 pack-3.2 oz poches per carton, 12 pack-3.2 oz poches per carton, 20 pack-3.2 oz poches per carton, 4 pack-3.2 oz poches per carton

Why the product was recalled

North Carolina Department of Health and Human Services (NCDHHS) sampled product and found it to contain high levels of lead.

Distribution information

Virginia, Kentucky, California, Puerto Rico, United Arab Emirates, Cuba

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly 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.

Related recall records

Other records from the same recalling company are shown first when available.