Food Recall Check
Class III · Low risk Terminated Initiated Apr 6, 2018 (9 years ago)

Italian Rose Garlic Spread recall

Recalled by Italian Rose Garlic Products, LLC · Riviera Beach, FL, United States

Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.

Why it was recalled

During a FDA inspection, it was disclosed that the firm is not documenting the mixing time of the product nor is pH monitoring for each kettle/batch mixed being conducted. The product is a shelf stable garlic spread.

See the recall's own reason text for the specifics. All other reasons recalls.

What was recalled

ITALIAN ROSE GARLIC SPREAD, Gluten Free, NET WT. 35 LB (16 kg), www.italian-rose.com, Riviera Beach, FL 33404

Quantity: 842 pails

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.

P-1-06517-6A, Exp Date 03/06/2018; P-1-06717-6A, Exp Date 03/08/2018; P-1-07417-7A, Exp. Date 03/15/2018; P-1-11717-11A, Exp Date 04/27/2018; P-1-12417-4A, Exp Date 05/04/2018; P-1-12917-4A, Exp Date 05/09/2018; P-1-15617-4D, Exp Date 06/05/2018; P-1-18017-4A, Exp Date 06/29/2018; P-1-20517-3A, Exp Date 07/24/2018; P-1-21317-1A, Exp Date 08/01/2018; P-1-25717-8A, Exp Date 9/14/2018; P-1-29417-1A, Exp. Date 10/21/2018; P-1-34317-3A, Exp Date 12/09/2018; P-1-35417-1A, Exp Date 2/20/2018; P-1-03218-5A, Exp Date 02/01/2019; P-1-05018-4A, Exp Date 02/19/2019

Where it was sold

Florida

FDA's distribution note: Florida consignees only.

Low risk, but check. Class III means the product is unlikely to make anyone ill but breaks an FDA rule, often a labeling one. If your package matches, the store will normally refund it. 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
Italian Rose Garlic Products, LLC
Initiated by
Voluntary: Firm initiated
Recall initiated
Apr 6, 2018
In FDA report of
May 2, 2018
Terminated
Aug 23, 2018
FDA recall number
F-1135-2018 · event 79823
Official record
FDA enforcement report search