Cole Slaw with Carrots Separate, 5 lb. bag, Dole brand. All marketed Dole and private label salads produced in the Springfield, OH fa...
⚠ Critical Alert — Stop Using Immediately
This product has been flagged with severe risks (other). 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-0688-2016.
Dole is suspending operations and withdrawing all marketed Dole and private label salads produced at the Springfield OH facility. Products may be identified with a product code beginning with the letter A in the upper right hand corner of the package.
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0688-2016.
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 Dole Fresh Vegetables Inc 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-0688-2016.
Dole Fresh Vegetables Inc
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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.
Dole Fresh Vegetables Inc Recall FAQ
Dole Fresh Vegetables Inc is the subject of a produce safety report: Cole Slaw with Carrots Separate, 5 lb. bag, Dole brand. All marketed Dole and private label salads produced in the Springfield, OH fa.... The notice was published on January 22, 2016 by the U.S. Food and Drug Administration (FDA). Approximately 0 units are potentially affected.