Food Recall Check
Class I · High risk Terminated Initiated Dec 14, 2016 (10 years ago)

Poppies Belgian Eclairs recall

Recalled by Poppie International INC · Battleboro, NC, United States

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

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

Pathogen: Salmonella

Salmonella is the most common cause of food recalls for bacteria, often in eggs, produce, nuts and spices.

The most serious food recalls: a contaminated product can cause outbreaks, hospitalisations and deaths, especially for pregnant people, young children, older adults and anyone with a weakened immune system. All bacteria & viruses recalls.

What was recalled

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

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

Lot Codes: L1H3216, L1I3216 and L1J3216.

Where it was sold

Arizona California Colorado Florida Hawaii Iowa Idaho Illinois Kansas Minnesota North Carolina New Jersey New York Ohio Oregon Pennsylvania Rhode Island Texas Utah Virginia Washington Wisconsin

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

Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm
Poppie International INC
Initiated by
Voluntary: Firm initiated
Recall initiated
Dec 14, 2016
In FDA report of
Jan 25, 2017
Terminated
Aug 3, 2017
FDA recall number
F-1282-2017 · event 76013
Official record
FDA enforcement report search

Also recalled with it (2 more products)

FDA files each product of one recall action separately; these share the same FDA event.