Recalls / Class I
Class IF-1634-2018
Product
Multiple Brands Mixed Melon: Customer Product Description Pack Weight UPC Label Description/Brand Caito Foods Disribution FRUIT BURST 4/20Z, 20 oz., UPC: 81851301409 Clear Generic Label Distributed by Caito Foods Caito Foods Disribution FRUIT BURST 6/10Z, 10 oz., UPC: 81851302215 Clear Generic Label Distributed by Caito Foods SpartanNash Distribution FRUIT BURST 6/10Z, 10 oz., UPC: 84853630887 Open Acres label SpartanNash Distribution FRUIT BURST 4/20Z, 20 oz., UPC: 84853630955 Open Acres label Sprouts FRUIT BURST 6/10Z , 10 oz., UPC: 646670522482 Sproutsouts Farmers Market label Walgreens FRUIT BURST 1/10Z, 10 oz., UPC: 49022558625 Delish label
- Type
- Food
- Affected lot / code info
- All products Best By or Use By: 4/27/18 to 6/16/18 Caito Foods Disribution FRUIT BURST 4/20Z, 20 oz., UPC: 81851301409 Clear Generic Label Distributed by Caito Foods Caito Foods Disribution FRUIT BURST 6/10Z, 10 oz., UPC: 81851302215 Clear Generic Label Distributed by Caito Foods SpartanNash Distribution FRUIT BURST 6/10Z, 10 oz., UPC: 84853630887 Open Acres label SpartanNash Distribution FRUIT BURST 4/20Z, 20 oz., UPC: 84853630955 Open Acres label Sprouts FRUIT BURST 6/10Z , 10 oz., UPC: 646670522482 Sproutsouts Farmers Market label Walgreens FRUIT BURST 1/10Z, 10 oz., UPC: 49022558625 Delish label
- Quantity
- 3,160,647.91 lbs. Total
Why it was recalled
Products have the potential to be contaminated with Salmonella.
Recalling firm
- Firm
- Caito Foods Service, Inc.
- Notification channel
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Type
- Voluntary: Firm initiated
- Address
- 3120 N Post Rd, Indianapolis, Indiana 46226-6514
Distribution
- Distribution pattern
- Domestic: AL, CA, FL, GA, IA, ID, IL, IN, KS, KY, MI, MN, MO, NC, ND, NE, OH, PA, SD, TN, VA, WI, WV
Timeline
- Recall initiated
- 2018-06-08
- FDA classified
- 2018-07-12
- Posted by FDA
- 2018-07-11
- Terminated
- 2018-10-18
- Status
- Terminated
Source: openFDA Food Enforcement endpoint. Recall record F-1634-2018. The FDA issues recall classifications as health-hazard assessments, not legal findings.