Charlie's brand perishable and refrigerated Spinach Salad With Honey Dijon Dressing, item # 028-09048, packaged in a cle
Summary
The FDA issued a Class II for Charlie's brand perishable and refrigerated Spinach Salad With Honey Dijon Dress by Triple B Corporation. Reason: Label declares Worcestershire Sauce but does not declare sub-ingredient fish (anchovy). The dressing, which contains Worcestershire sauce and sub-ing.
Details
Source
Food Recall
External ID
F-1687-2022
Action Date
2022-09-14
Status
Terminated
Category
food
Product Description
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***".
Lot/Code Info: USE BY OF 5/1/2022-8/10/2022
Quantity Affected: 4438 containers
Reason for Recall
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.
Distribution
Distributed in Idaho, Montana, Oregon, and Washington.
Type: Voluntary: Firm initiated
Recall Initiated: 2022-08-08
Company
Seattle, WA
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 129 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Triple B Corporation has 2 FDA actions in our database, including 2 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Triple B Corporation) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Triple B Corporation have FDA actions?
Triple B Corporation has 2 FDA actions in our database, including 2 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1687-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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