Food Recall Check
Class II · Moderate risk Terminated Initiated Jan 15, 2013 (14 years ago)

Dried Preserved Plum packaged in clear recall

Recalled by Nuera Trading Company Incorporated · San Leandro, CA, United States

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

Why it was recalled

California Department of Public Health sampled Dried Plum Preserves in 4.4 lb packages and found it to contain lead at 1.5 and 1.6 ug/g.

Some of these cause harm only with repeated exposure (lead in spices, for example), others act within hours (histamine poisoning from spoiled fish). All chemical contamination recalls.

What was recalled

Dried Preserved Plum packaged in clear 4.4 lb (1904 g) plastic packages. The product comes in bulk form in a brown corrugated box with 10 x 4.4 lb packages. Net weight of one case is 44 lbs.. Product information is provided on the case with product name "Dried Preserved Plum" and Net Weight 44 lbs. (Product was destroyed and photos of product are not available). Distributed by Nuera Trading Company Inc., San Leandro, CA. Manufactured by Zi Jing Yuk Hin Enterprises, Guangdong, China.

Quantity: ~580 cartons (10 x 4.4lb packages per carton)

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.

No code information

Where it was sold

California New York Texas Washington

FDA's distribution note: CA, WA, TX and NY

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
Nuera Trading Company Incorporated
Initiated by
Voluntary: Firm initiated
Recall initiated
Jan 15, 2013
In FDA report of
Feb 13, 2013
Terminated
Aug 19, 2013
FDA recall number
F-0968-2013 · event 64179
Official record
FDA enforcement report search

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