Food Recall Check
Class II · Moderate risk Terminated Initiated Sep 30, 2014 (12 years ago)

Outer Carton labeled in part as recall

Recalled by Multiple Organics, Inc. · Hercules, CA, United States

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

Why it was recalled

Firm was notified that the product may contain fragments of metal that if ingested, may be injurious to human health. Firm has not been able to independently verify the reports, but believes it prudent to take this action.

Hard or sharp fragments can cut the mouth or throat, break teeth or cause choking. They usually come from equipment wear or packaging on the production line. All foreign material recalls.

What was recalled

Outer Carton labeled in part as: Multiple Organics Certified 100% Organic Mango Fillets Net Weight 20 Lbs. (9.07 kgs) In 5 X 4 Lb. bags Product of Mexico Certified Organic by QAI www.multipleorganics.com USDA Organic Inner plastic bag labeled in part as: Organic Mango Filets Net Weight 5Lbs (2.26 kgs) Product of Mexico Certified Organic by QAI www.multipleorganics.com 209 Linus Pauling Dr., Hercules, CA 94547

Quantity: 687 / 20 Lb. cartons

Food: Fresh fruit

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.

Organic lot #s 12030614, 12180614, 12100614, 12230614 Dates of production are 6/3/2014, 6/18/2014, 6/10/2014 and 6/23/2014 Item Code 2-MA-20-24073 No UPC codes

Where it was sold

FDA's distribution note: U.S. Distribution. No Foreign.

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
Multiple Organics, Inc.
Initiated by
Voluntary: Firm initiated
Recall initiated
Sep 30, 2014
In FDA report of
Oct 29, 2014
Terminated
Dec 29, 2014
FDA recall number
F-0059-2015 · event 69390
Official record
FDA enforcement report search

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