Food Recall Check
Class II · Moderate risk Terminated Initiated Dec 27, 2012 (14 years ago)

Deep Best Quality Dry Garlic Chutney recall

Recalled by Deep Foods Inc · Union, NJ, United States

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Unapproved dye in product (Rhodamine B - Basic Violet 10).

These are failures of the safety steps that keep food safe - cooking, pasteurising, keeping cold, sealing - even when no contaminant has yet been found. All processing & sanitation problems recalls.

What was recalled

Deep Best Quality Dry Garlic Chutney (Thechaa); Net Wt. 4 OZ.; UPC 011433111201; Deep Foods, Inc. Union, NJ 07083

Quantity: 7000 units per month

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 011433111201

Where it was sold

Alabama Arizona California Colorado Connecticut Delaware Florida Georgia Idaho Illinois Louisiana Massachusetts Maryland Maine Missouri Mississippi North Carolina New Hampshire New Jersey New York Ohio Pennsylvania Rhode Island South Carolina Tennessee Virginia West Virginia

FDA's distribution note: 27 states (Alabama, Arizona, California, Colorado, Connecticut, Delaware, Florida, Georgia, Idaho, Illinois, Louisiana, Massachusetts, Maryland, Maine, Mississippi, Missouri, North Carolina, New Hampshire, New Jersey, New York, Ohio, Pennsylvania, Rhode Island, South Carolina, Tennessee, Virginia and West Virginia.

Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. 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
Deep Foods Inc
Initiated by
Voluntary: Firm initiated
Recall initiated
Dec 27, 2012
In FDA report of
Mar 13, 2013
Terminated
Aug 6, 2013
FDA recall number
F-1051-2013 · event 64284
Official record
FDA enforcement report search

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