Charlie's brand perishable and refrigerated Spinach Salad With Honey Dijon Dr...
FDA Recall #F-1687-2022 — Class II — August 8, 2022
Recall Summary
| Recall Number | F-1687-2022 |
| Date Initiated | August 8, 2022 |
| Classification | Class II |
| Status | Terminated |
| Type | Voluntary: Firm initiated |
| Product Type | Food |
Recalling Firm
| Firm | Triple B Corporation |
| Location | Seattle, WA |
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***".
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.
Classification
Class II — A situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
Distribution Pattern
Distributed in Idaho, Montana, Oregon, and Washington.
Product Quantity
4438 containers
Product Codes / Lot Numbers
USE BY OF 5/1/2022-8/10/2022
What Should You Do?
Stop consuming this product immediately. Check your home for the recalled item and dispose of it safely. If you experienced a health issue after consuming this product, contact your doctor and report it to the FDA MedWatch.
Frequently Asked Questions
Stop consuming the product immediately and do not donate or give it to others. Check the recall notice above for specific disposal or return instructions. Many food recalls ask you to throw the product away and retain the packaging for a possible refund from the retailer. If you purchased it online, check your order history — some retailers send recall notifications directly to customers. You do not need a receipt to report an issue or seek a refund; the fact of purchase is typically sufficient.
In most cases, yes. Retailers are typically notified to accept returns of recalled products and issue refunds, regardless of whether you have a receipt. Check with the store where you purchased the item. Some manufacturers also offer direct refunds — contact the recalling firm using the information in the official recall notice. If you purchased the product online, contact the retailer's customer service with your order number. In either case, you generally do not need original packaging, though retaining the product label with the lot code or UPC can speed up the process.
Report foodborne illnesses and adverse food reactions to the FDA through the MedWatch Safety Reporting Portal at FDA.gov, or by calling 1-800-332-1088. You can also report issues directly to the FDA's Safety Reporting Portal at SafetyReporting.hhs.gov. If you believe there is an immediate public health risk, contact your local health department. Your report helps the FDA identify contamination patterns, initiate recalls faster, and protect other consumers from the same hazard. Include as much detail as possible: the product name, lot code, purchase date and location, and a description of your symptoms or findings.
The FDA assigns a status to each recall action throughout its lifecycle. "Ongoing" means the recall is active — the firm is still working to remove the product from commerce and notify consumers. "Completed" means the recall strategy has been implemented and the FDA has determined that the recalling firm has taken all appropriate steps to remove the product. "Terminated" means the FDA has reviewed the results and concluded the recall is complete. Even if a recall is marked as completed or terminated, you should still discard any recalled products you find at home — the recall status refers to the firm's compliance actions, not the safety of product still in consumers' possession.