Dole Colourful Coleslaw
Reason Complaints received of irregular pieces of soft plastic in the product.
Dole Classic Coleslaw recall
Recalled by Dole Fresh Vegetables · Monterey, CA, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Complaints received of irregular pieces of soft plastic in the product.
Hard or sharp fragments can cut the mouth or throat, break teeth or cause choking. They usually come from equipment wear or packaging on the production line. All foreign material recalls.
What was recalled
Dole Classic Coleslaw (US) Shredded cabbage and carrots. 14 oz. US
Quantity: 6255 cases of Classic Coleslaw (US)
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
Lot numbers for Classic Coleslaw (US) include: B10203A, B10203B, B1024A, B1024B with Use By date of 5-2-19
Where it was sold
Alabama Arizona California Colorado Florida Iowa Idaho Illinois Kansas Kentucky Louisiana Massachusetts Maryland Michigan Minnesota Missouri Mississippi North Carolina North Dakota Nebraska New York Ohio Oregon Pennsylvania South Carolina Tennessee Texas Utah Virginia Washington Wisconsin
FDA's distribution note: US: AL, AZ, CA, CO, FL, IA, ID, IL, KS, KY, LA, MA, MD, MI, MN, MO, MS, NC, ND, NE, NY, OH, OR, PA, SC, TN, TX, UT, VA, WA, WI. Colorful Coleslaw (Canada): AB, BC, SK
Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- Dole Fresh Vegetables
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- May 2, 2019
- In FDA report of
- Jun 5, 2019
- Terminated
- Jun 3, 2019
- FDA recall number
- F-1424-2019 · event 82757
- Official record
- FDA enforcement report search
Also recalled with it (1 more product)
FDA files each product of one recall action separately; these share the same FDA event.
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