Food Recall Check
Class I · High risk Terminated Initiated Feb 3, 2016 (11 years ago)

Margaritaville recall

Recalled by Jel Sert Co. · West Chicago, IL, United States

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

Why it was recalled

There was a positive salmonella sample from another customer of the supplier that tested it. This firm uses the freeze dried bananas in their Banana creme pie filling mix.

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

Margaritaville 4.16 ounce packages of Banana creme pie filling mix packaged in a yellow, red, and blue box with white lettering.

Quantity: 65 cases, 8 boxes/case.

Food: Bread & bakery

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 Code: WC5257 Best before Sept 2017 Universal Product Code: 7239202925

Where it was sold

FDA's distribution note: 65 cases were used for sales samples and gifts. Of those cases (520 cartons) ~ 20 cartons are not accounted for and were most likely given to employees and or consumed. 17 other cases were used by Marketing and R&D.

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
Jel Sert Co.
Initiated by
Voluntary: Firm initiated
Recall initiated
Feb 3, 2016
In FDA report of
Jul 6, 2016
Terminated
Feb 26, 2018
FDA recall number
F-1594-2016 · event 73217
Official record
FDA enforcement report search

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