Home / Food recalls / 2022
Triple B Corporation
FDA recall F-1687-2022 · Class II · reported 2022-09-14 · Terminated
- Product
- Charlie's brand perishable and refrigerated Spinach Salad With Honey Dijon Dressing, item # 028-09048, packaged in a clear hinged container, net weight per container: 6 oz. UPC 0 45009 85415 5. There are 8/6oz. Spinach Salad With Honey Dijon Dressing containers in the Spinach Salad master case. UPC on master case is 45009 85415 5. There are 2/6oz. Spinach Salad With Honey Dijon Dressing containers in the Charlie's Salad Variety Pack. UPC on master case is 45009 85417 9. There are three other types of salad in this master case but they are not subject to recall. The salad dressing, which contains Worcestershire sauce and sub-ingredient anchovy, is packaged in a small plastic cup with a plastic film lid. The plastic cup displays a USE BY Date, a Production Time Stamp, and the identifier of the Dressing Type: DIJON. The 6 oz. Spinach Salad With Honey Dijon Dressing label is read in parts: "***Ingredients: Spinach, Honey Mustard Dressing (Soybean or Canola Oil, Water, Mustard*** Eggs ***Worcestershire Sauce (Apple Cider Vinegar, Water, Molasses, Tamari [Water, Soybeans, Salt, Alcohol, Koji]***Contains: Egg, Soy***Produced by: CP Fresh, PO Box 24606, Seattle, WA 98124***".
- Reason
- Label declares Worcestershire Sauce but does not declare sub-ingredient fish (anchovy). The dressing, which contains Worcestershire sauce and sub-ingredient anchovy, is packaged in a small cup in the Spinach Salad container.
- Quantity
- 4438 containers
- Distribution
- Distributed in Idaho, Montana, Oregon, and Washington.
- Firm location
- WA, United States
- Initiated
- Voluntary: Firm initiated
- First notice
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Recall started
- 2022-08-08
- Terminated
- 2022-09-26
- Code info
- USE BY OF 5/1/2022-8/10/2022
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.