10-inch Supreme Chocolate Layered Cake
Reason Foreign Material Contamination - Ball point pen
10" Chocolate Supreme Cake Layers recall
Recalled by CSM Bakery Products North America · Dallas, TX, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Foreign Material - specifically the product has the potential to contain pieces of a red plastic scoop.
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
10" Chocolate Supreme Cake Layers, NET WT. 20 oz. packed in cases of 12. Keep Frozen until ready to use. CSM Bakery Products NA, Inc., Tucker, GA 30084 USA Product is for institutional use.
Quantity: 576 cases each containing 12 - 20 oz. cake layers
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 #1328702013 All cases stamped with Lot #1328702013 and also showing a USE BY date of JUL/14/14 along with a 24-hour time stamp between 15:00 and 24:00. For example, a case showing "1328702013 17:36 USE BY JUL/14/14" is subject to the recall while "1328702013 02:14 USE BY JUL/14/14" is not subject to the recall. Also NOT included in the recall would be a case showing an earlier USE BY date along with Lot # 1328702013. For example, "1328702013 15:36 USE BY JUL/13/14" is not subject to the recall.
Where it was sold
Illinois Wisconsin
FDA's distribution note: Illinois and Wisconsin
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
- CSM Bakery Products North America
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Nov 20, 2013
- In FDA report of
- Mar 26, 2014
- Terminated
- May 12, 2014
- FDA recall number
- F-1681-2014 · event 66928
- Official record
- FDA enforcement report search
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