FDA recall record

Giant Eagle GE 22985000000 Petite Cake Peanut Butter 18Oz recall — FDA F-1392-2022

Products were made with Jiff Peanut Butter and have the potential for Salmonella Contamination.

Class Iclassification
F-1392-2022official record ID
Jul 13, 2022report date

Recall record at a glance

Official recordF-1392-2022
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmGiant Eagle
Report dateJul 13, 2022
Recall initiation dateMay 23, 2022
Quantity5 Units
LocationPittsburgh, PA, United States

Official product description

GE 22985000000 Petite Cake Peanut Butter 18Oz

Why the product was recalled

Products were made with Jiff Peanut Butter and have the potential for Salmonella Contamination.

Distribution information

The product was distributed domestically to the following State: PA

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.

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