J.M. Rosen's Cheesecake
Reason Retail store employee noticed a small rubber object in the cheesecake - the firm is recalling the entire day's production.
J.M. Rosen's Cheesecake recall
Recalled by J.M.Rosen Cheesecake · Petaluma, CA, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Retail store employee noticed a small rubber object in the cheesecake - the firm is recalling the entire day's production.
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
J.M. Rosen's Cheesecake - New York Traditional; 6 - Unit- 4/46 oz in a case box; Product #56378 UPC 6 93892 99462 7; INGREDIENTS: Cream Cheese (Pasteurized Nonfat Milk, and Milkfat~ Whey Protein Concentrate, Cheese Culture. Salt, Whey, Stabilizers (Xanthan Gum, and/or Carob Bean Gum, and/or Guar Gum)}, Unbleached Flour, (Unbleached Wheat Flour, Thiamine Mono-nitrate, Niacin. Iron, Riboflavin, Folic Acid, Malted Barley Flour), Granulated Sugar Cane, Eggs, Unsalted Butter (Cream {Milk)), Sour Cream (Milk, Enzymes). Cream {Milk), Orange and Lemon Rind, Nielson Massey Vanilla).
Quantity: 119 cases
Food: Cheese
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.
6 New York B6-22218 / B7-22218 /B8-22218/ B9-22218
Where it was sold
California Hawaii Nevada
FDA's distribution note: One distributor in CA and to retail stores in CA, HI, NV.
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
- J.M.Rosen Cheesecake
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Mar 16, 2018
- In FDA report of
- Apr 4, 2018
- Terminated
- Mar 29, 2018
- FDA recall number
- F-0973-2018 · event 79578
- 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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