Carnival Cauli Florets, 6/16 oz., RETAIL item # 73633, New Seasons Market brand, UPC 10200 24467. Ingredients: Green Cauliflower, Ora...
⚠ Critical Alert — Stop Using Immediately
This product has been flagged with severe risks (listeria). Stop using it now and contact the brand or FDA for a refund, repair, or replacement.
FDA Recall Notice
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0041-2018.
Pacific Coast Fruit Company, Portland, Oregon is voluntarily recalling multiple types of bagged processed salads based on the potential contamination of Listeria monocytogenes. The firm utilized a portion of the salads that were recalled by their supplier.
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0041-2018.
Recall terminated by FDA.
✅ What you should do
- Stop using the product if you own it.
- Check the model number, lot code, or sell-by date against the recall notice above.
- Contact Pacific Coast Fruit Company or the retailer where you bought it for a refund, replacement, or repair.
- For the most current official instructions, visit the FDA recall page.
- If you've been hurt by this product, report the incident to FDA.
Consumer Contact (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0041-2018.
Pacific Coast Fruit Company
About the U.S. Food and Drug Administration
The FDA regulates drugs, medical devices, food, cosmetics, and tobacco. Adverse event reports and recall notices are the main public safety signal.
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If you had a reaction, found contamination, or experienced a labeling problem with this product, report it to the FDA. The agency uses consumer reports to track emerging safety signals and trigger recalls.
Pacific Coast Fruit Company Recall FAQ
Pacific Coast Fruit Company is the subject of a food safety report: Carnival Cauli Florets, 6/16 oz., RETAIL item # 73633, New Seasons Market brand, UPC 10200 24467. Ingredients: Green Cauliflower, Ora.... The notice was published on October 20, 2017 by the U.S. Food and Drug Administration (FDA). Approximately 40 units are potentially affected.