Recalls / Class I
Class IF-1625-2018
Product
Honeydew, Clear Generic Label Distributed by Caito Foods; distributed at Gordon Food Service, Clear Generic Label Distributed by Caito Foods Distributed at Kroger with Clear Generic Label Distributed by Renaissance Food Group Distributed at SpartanNash Distribution with Open Acres labeling; Sproutsouts Farmers Market; Distributed by Trader Joe's with Trader Joe's Labeling Distributed at Walgreens with Delish labeling Distributed at Walmart with Freshness Guaranteed labeling Distributed by Whole Foods/Amazon with Whole Foods Market labeling
- Type
- Food
- Affected lot / code info
- All products Best By or Use By: 4/27/18 to 6/16/18 Brands Distributed: Caito Foods LLC, Renaissance Food Group, Open Acres, Sproutsouts Farmers Market, Delish, Freshness Guaranteed, and Whole Foods Market, Trader Joes Cantaloupe, Clear Generic Label Distributed by Caito Foods; distributed at Gordon Food Service, Clear Generic Label Distributed by Caito Foods Distributed at Kroger with Clear Generic Label Distributed by Renaissance Food Group Distributed at SpartanNash Distribution with Open Acres labeling; Sproutsouts Farmers Market; Distributed at Walgreens with Delish labeling Distributed at Walmart with Freshness Guaranteed labeling Distributed by Whole Foods/Amazon with Whole Foods Market labeling
- 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-1625-2018. The FDA issues recall classifications as health-hazard assessments, not legal findings.