Food Recall Check
Class I · High risk Terminated Initiated Oct 3, 2015 (11 years ago)

Skinny Latina Million Dollar Marinade recall

Recalled by Skinny Latina LLC · Coral Gables, FL, United States

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

Why it was recalled

Undeclared soy

Undeclared allergen: Soy

For someone with a food allergy the label is the only protection. An undeclared allergen can trigger a severe reaction even in a trace amount, which is why most of these recalls are Class I. All undeclared allergens recalls.

What was recalled

Skinny Latina Million Dollar Marinade, 12 oz, shelf stable, dry storage.

Quantity: 18,822 bottles

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.

UPC #8-55329-00400-6; Lots 12/02/15A, 12/02/15B, 10/21/15A, 10/21/15B, 10/22/15A, 10/22/15B, 10/23/15A, 10/23/15B, 10/24/15A, 10/24/15B, 10/28/15A, 10/28/15B, 10/27/15A, 10/27/15B, 10/29/15A, 10/29/15B

Where it was sold

Nationwide.

Florida

FDA's distribution note: Distributed to distribution centers and retail stores nationwide. Distributed to KeHe distribution centers which distribute product to Target stores and WholeFood stores nationwide. Skinny Latina, LLC directly ships to Fresh Market stores in Florida.

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. The risk from an undeclared allergen is to people allergic to soy; for anyone else the product is generally not a safety concern. 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
Skinny Latina LLC
Initiated by
Voluntary: Firm initiated
Recall initiated
Oct 3, 2015
In FDA report of
Jan 13, 2016
Terminated
Feb 13, 2017
FDA recall number
F-0464-2016 · event 72508
Official record
FDA enforcement report search