Recall record at a glance
| Official record | F-0969-2013 |
|---|---|
| Category | Food Recalls |
| Classification | Class III |
| FDA record status | Terminated |
| Recalling firm | Acme Food Sales, Inc. |
| Report date | Feb 13, 2013 |
| Recall initiation date | Nov 30, 2012 |
| Quantity | 8707 cs (24 cans/cs) |
| Location | Seattle, WA, United States |
Official product description
Canned mandarin oranges labeled in part: "WESTERN FAMILY Choice Selections Mandarin Oranges Naturally Sweet in Mandarin Orange Juice NET WT 10.5OZ (297g)***Ingredients: Mandarin Oranges, Mandarin Orange Juice. Proudly Distributed by Western Family P.O. Box 4057, Portland, OR 97208 U.S.A.***Product of China***0 15400 01241 6***"
Why the product was recalled
The firm received two consumer complaints regarding chemical smell/taste and tasting like the can. As a result the firm began extensive testing of its inventory. Preliminary testing identified a contaminant was present. Further testing is pending to specifically identify the contaminant.
Distribution information
The product was distributed to one wholesaler - Associated Food Stores (AFS) Farr West, Far West, Utah. The January 31, 2015 code was first not thought to have been distributed to retail, however; Associated Food Stores corrected this information and issued a second recall notice because the product had been distributed from their warehouse to retail. Lot codes with Best Buy: DEC 15 2014 and DEC 15 2014 were not distributed out of Acme's warehouse and are currently under their control.
How to read the classification
FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken from the FDA enforcement record.
Additional record details
Recall type: Voluntary: Firm initiated. Initial notification: Telephone.
What to do next
If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.
About this record
Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.
FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.