FDA recall record

Poppie International Net Wt recall — FDA F-1282-2017

Product contains milk product from a supplier that is recalling product due to the possible presence of Salmonella.

Class Iclassification
F-1282-2017official record ID
Jan 25, 2017report date

Recall record at a glance

Official recordF-1282-2017
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmPoppie International Inc.
Report dateJan 25, 2017
Recall initiation dateDec 14, 2016
LocationBattleboro, NC, United States

Official product description

Poppies Belgian Eclairs,Net Wt. 710 g/25 oz., Contents 50 ct. Mini Eclairs, UPC Code: 0 08563 10710 5.

Why the product was recalled

Product contains milk product from a supplier that is recalling product due to the possible presence of Salmonella.

Distribution information

AZ, CA, CO, FL, HI, IA, ID, IL, KS, MN, NC, NJ, NY, PA, OH, OR, RI, TX, UT, VA, WA and WI

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: E-Mail.

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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