FDA recall record

Caito Foods Service Multiple Brands Mixed Melon: Customer Product Description Pack recall — FDA F-1638-2018

Products have the potential to be contaminated with Salmonella.

Class Iclassification
F-1638-2018official record ID
Jul 11, 2018report date

Recall record at a glance

Official recordF-1638-2018
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmCaito Foods Service, Inc.
Report dateJul 11, 2018
Recall initiation dateJun 8, 2018
Quantity3,160,647.91 lbs. Total
LocationIndianapolis, IN, United States

Official product description

Multiple Brands Mixed Melon: Customer Product Description Pack Weight UPC Label Description/Brand Caito Foods Disribution FRUIT MIX 6/10Z, 10 oz., UPC: 81851301348 Clear Generic Label Distributed by Caito Foods Caito Foods Disribution FRUIT MIX 6/5Z, 5 oz., UPC: 81851301393 Clear Generic Label Distributed by Caito Foods Caito Foods Disribution FRUIT MIX 3/48Z , 48 oz., UPC: 81851301416 Clear Generic Label Distributed by Caito Foods Caito Foods Disribution FRUIT MIX 6/16Z, 16 oz., UPC: 81851301447 Clear Generic Label Distributed by Caito Foods Caito Foods Disribution FRUIT MIX 1/5LB, 80 oz., UPC:81851302079 Clear Generic Label Distributed by Caito Foods Gordon Food Service FRUIT MIX 6/4.5Z, 4.5 oz., UPC: 826766257676 Clear Generic Label Distributed by Caito Foods SpartanNash Distribution FRUIT MIX 6/5Z, 5 oz., UPC: 884853630610 Open Acres label SpartanNash Distribution FRUIT MIX 6/10Z,10 oz., UPC: 884853630900 Open Acres label SpartanNash Distribution FRUIT MIX 3/48Z , 48 oz., UPC: 884853630962 Open Acres label SpartanNash Distribution FRUIT MIX 6/16Z, 16 oz., UPC: 884853630993 Open Acres label Walgreens FRUIT MIX 1/10Z 10 oz., UPC: 49022822443 Delish label

Why the product was recalled

Products have the potential to be contaminated with Salmonella.

Distribution information

Domestic: AL, CA, FL, GA, IA, ID, IL, IN, KS, KY, MI, MN, MO, NC, ND, NE, OH, PA, SD, TN, VA, WI, WV

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

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.

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