Recall record at a glance
| Official record | F-2365-2012 |
|---|---|
| Category | Food Recalls |
| Classification | Class I |
| FDA record status | Terminated |
| Recalling firm | Triple B Corporation - Charlie's Produce |
| Report date | Sep 26, 2012 |
| Recall initiation date | Aug 30, 2012 |
| Quantity | 1) 193 cs; 2) 361 cs (6 pk/cs) |
| Location | Seattle, WA, United States |
Official product description
Fruit Bowls: 1) Seasonal Fruit Bowl (Walmart) Item # 028-06480***" and the UPC of the package is 0 45009 06480 6 and Case UPC is 0 45009 06480 6. Case label reads in part "***ALASKA CARROT Seasonal Fruit Bowl 6/40 oz *** Packed By: Charlie's Produce, Anchorage, AK***" Use By 7/21/12 through 8/31/12; Package label reads in part "*** Fruit Bowl Gold Pineapple, Cantaloupe, Red Grapes, Strawberry Mango and Kiwi *** PRODUCT OF: Blueberry: USA Strawberry: Mexico Mango: Mexico Kiwi: New Zealand 2) Gourmet Fruit Bowl has the Item # 028-006693, and UPC 6 97327 06693 4. Label reads in part "*** ALASKA CARROT *** FRESH Sliced FRUIT *** ANCHORAGE, AK***" "*** 64oz Gourmet Fruit Bowl Gold Pineapple, Cantaloupe, Red Grapes, Strawberry Mango and Kiwi***" "PRODUCT OF: Pineapple - COSTA RICA Cantaloupe - USA Red Grapes - USA Mangoes - Mexico Kiwi - NEW ZELAND Strawberry - USA ***" "*** Packed By: Charlie's Produce, Anchorage, AK***".
Why the product was recalled
Daniella brand mangos are recalled because they have the potential to be contaminated with Salmonella.
Distribution information
Distributed in Alaska and Washington.
How to read the classification
FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly 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
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