Food Recall Check
Class III · Low risk Terminated Initiated Mar 11, 2016 (11 years ago)

Imperial Choice Mandarin Oranges Broken Segments in Light Syrup recall

Recalled by Greater Pittsburgh Community Food Bank · Duquesne, PA, United States

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

Why it was recalled

Greater Pittsburgh Community Food Bank is announcing a voluntary recall of one lot of Imperial Choice Mandarin Oranges Broken Segments in Light Syrup because some of the cans from this lot may leak, bulge or burst open. The product may be contaminated by spoilage organisms or pathogens, which could lead to serious or life threatening illness if consumed. This recall only affects cans marked with code 4200/01029.

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

Imperial Choice Mandarin Oranges Broken Segments in Light Syrup; Net WT. 11 oz.; Imported by Acme Food Sales, Seattle, WA 98108; Product of China; 4200/01029; PRO: DEC 21, 2013; Best By: Dec 21, 2016

Quantity: 2200 cases (cans per case unk.)

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.

On can end: 4200/01029; PRO: DEC 21, 2013; Best By: Dec 21, 2016

Where it was sold

Pennsylvania

FDA's distribution note: Southwest PA

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
Greater Pittsburgh Community Food Bank
Initiated by
Voluntary: Firm initiated
Recall initiated
Mar 11, 2016
In FDA report of
May 18, 2016
Terminated
Mar 6, 2017
FDA recall number
F-1245-2016 · event 73702
Official record
FDA enforcement report search