Wildwood Emerald Valley Kitchen Organic Medium Salsa recall

Recalled by Pulmuone Wildwood Inc · Fullerton, CA, United States

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

Why it was recalled

The firm recalled due to a potential non-safety quality concern related to a particular ingredient that was causing premature spoilage.

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

Wildwood Emerald Valley Kitchen Organic Medium Salsa, 30 oz. Pack size 6/30 oz per case, 14 oz Pack size 6/14oz per case, Packaged in plastic cup, sealed with film and capped with plastic cap. Product labeling reads in part:" WILDWOOD Emerald Valley KITCHEN ORGANIC MEDIUM SALSA***MANUFACTURED BY PULMUONE FOODS USA, Inc. Fullerton, CA 92833***"

Quantity: 61,288 units

Food: Sauces, dips & dressings

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 0-52334-11665-0, Item # 0291623. UPC 0-52334-11653-7, Item # 0291638

Where it was sold

Nationwide.

FDA's distribution note: Nationwide and Canada.

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: Pulmuone Wildwood Inc
Initiated by: Voluntary: Firm initiated
Recall initiated: Jul 12, 2012
In FDA report of: Oct 3, 2012
Terminated: Dec 17, 2012
FDA recall number: F-2433-2012 · event 62991
Official record: FDA enforcement report search

Also recalled with it (6 more products)

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

Class II · Moderate risk Terminated Processing Jul 12, 2012