Recall record at a glance
| Official record | F-0029-2013 |
|---|---|
| Category | Food Recalls |
| Classification | Class I |
| FDA record status | Terminated |
| Recalling firm | Cut Fruit Express, Inc. |
| Report date | Oct 17, 2012 |
| Recall initiation date | Sep 13, 2012 |
| Quantity | 372 Cases total |
| Location | Inver Grove Heights, MN, United States |
Official product description
CANTALOUPE, HONEY DEW, PINEAPPLE AND GRAPES (CHPG) UNDER THE FOLLOWING BRANDS: Indianhead Foods 13105 FRUIT MIX CHPG 5# Manufactured by Cut Fruit Express Mpls, MN 55076 Following products Distributed by H. Brooks & Co. Mpls, MN 55112: H.Brooks & Company 31165 MIXED FRUIT CHPG 4/16OZ 16oz 4 per case UPC# 0 3823231165 6. Festival Foods-Best Of The Season 31165 MIXED FRUIT CHPG 4/16OZ 16oz 4 per case UPC# 0 3823231165 6. Kitchen Cravings Kwik Trip #1 31595 FRUIT CUP MIX Chunks 5.5oz 24 per case UPC# 0 3977955262 5. Kitchen Cravings Kwik Trip #31616 Fruit Tray 16 oz 12 per case UPC#0 3977955265 6. Supermom's /Super America-Goodies-to go! 31595 FRUIT MIX CHPG 5.5 oz 24 per case UPC# 76391390250 1. H.Brooks 34382 MIXED FRUIT CHPG Net Wt 8 oz(227g) 6 per case 19 UPC# 0 3823234382 4. H.Brooks 37663 FRUIT MIXED CHPG Net Wt 12oz(340g) 4 per case 175 UPC# 0 3823237663 1.
Why the product was recalled
Cut Fruit Express, Inc processed cantaloupe that was later recalled by the supplier DFI Marketing due to a positive Salmonella sample.
Distribution information
MI, MN, WI
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: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.
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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