Hexing Haw Balls candy
Reason Unapproved dye Ponceau 4R
Ideal Protein Double Chocolate Brownie recall
Recalled by Laboratories Cop Inc · Gatineau, Quebec, Canada
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Possible contamination with thin metal fragments.
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
Ideal Protein Double Chocolate Brownie. Individually wrapped, sold in boxes of 7.
Quantity: 54,060
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: 30213, 30913, 31113, 31613, 31813, 32313, 33213, 02814, 03614
Where it was sold
Nationwide.
Alaska Arkansas Arizona California Colorado Connecticut Delaware Florida Georgia Iowa Idaho Illinois Indiana Kansas Louisiana Massachusetts Maryland Maine Michigan Minnesota Missouri Mississippi Montana North Carolina North Dakota Nebraska New Hampshire New Jersey New Mexico Nevada New York Ohio Oklahoma Oregon Pennsylvania Puerto Rico Rhode Island South Carolina South Dakota Tennessee Texas Utah Virginia Vermont Washington Wisconsin West Virginia Wyoming
FDA's distribution note: Nationwide: AK, AR, AZ, CA, CO, CT, DE, FL, GA, IA, ID, IL, IN, KS, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, WY
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
- Laboratories Cop Inc
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Feb 20, 2014
- In FDA report of
- Apr 9, 2014
- Terminated
- Jul 2, 2015
- FDA recall number
- F-1741-2014 · event 67649
- Official record
- FDA enforcement report search
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