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Diamond Crystal Brands, Inc.
FDA recall F-0863-2019 · Class I · reported 2019-02-20 · Terminated
- Product
- Vanilla instant pudding and pie filling packaged in the following ways: 1) Classic Sysco Vanilla Instant Pudding & Pie Filling Mix, Net Wt. 24 OZ, Distributed by Sysco Corporation, Houston, TX, in paper pouches, 12 per case; 2) Classic Sysco Vanilla Instant Pudding & Pie Filling Mix, Net Wt. 32 OZ, Distributed by Sysco Corporation, Houston, TX, in paper pouches, 12 per case; 3) Ellington Farms, Vanilla Instant Pudding & Pie Filling, Net Wt. 24 OZ, Distributed By Ben E. Keith Foods, Fort Worth, TX, in paper pouches, 12 per case; 4) Chef's Companion, Vanilla Instant Pudding & Pie Filling, Net Wt. 24 OZ, Distributed by Diamond Crystal Brands, Inc, in paper pouches, 12 per case; 5) Katy's Kitchen, Instant Pudding Mix, Vanilla, Net Wt. 24 OZ, Marketed by Independent Marketing Alliance, Houston, TX, in paper pouches, 12 per case; 6) Monarch, Vanilla Pudding & Pie Filling Mix, Net Wt. 24 OZ, Distributed by US Foods, Inc. Rosemont, IL, in paper pouches, 12 per case;
- Reason
- Recalled products were manufactured with an ingredient that is potentially contaminated with Salmonella.
- Quantity
- 8,314 cases
- Distribution
- Product shipped to distributors in the following US states: AL, AR, AZ, CA, CO, CT, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, SC, SD, TN, TX, UT, VA, WA, and WI
- Firm location
- GA, United States
- Initiated
- Voluntary: Firm initiated
- First notice
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Recall started
- 2019-01-04
- Terminated
- 2019-07-19
- Code info
- 309JCA, November 5, 2020; 310JCA, November 6, 2020; 311JCA, November 7, 2020; 318JDA, November 14, 2020; 323JDA, Exp November 19, 2020; 324JDA Exp November 20, 2020; 325JDA, Exp November 21, 2020
Source: U.S. Food and Drug Administration, openFDA Food Enforcement database (openFDA Food Enforcement, imported 2026-09). The FDA does not validate openFDA data for completeness or accuracy. This is a record of an enforcement action, not safety advice.