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Lower risk Food recall · FDA · Published March 16, 2018

J.M. Rosen Cheesecake Recall: Small Rubber Object Found in Product

J.M. Rosen is recalling New York Traditional Cheesecake due to a small rubber object found in the product. This recall affects 6 units of 4/46 oz cheesecake sold in case boxes with specific UPC and product numbers.

🇺🇸 FDA recall #F-0973-2018FoodJ.M. Rosen ›
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Contact the company

Recalling firmJ.M.Rosen Cheesecake74 E Washington St · Petaluma, CA 94952-3165
✎ GovInfoNow plain-language explainer

What happened, in plain English

J.M. Rosen is recalling all New York Traditional Cheesecake products made that day because a retail employee found a small rubber object in the cheesecake. This recall is for safety as the rubber object could pose a choking hazard for young children. Read more at govinfonow.com/recall/19536-j-m-rosen-cheesecake-recall-small-rubber-object-found-in.

Source Summary by GovInfoNow · govinfonow.com/recall/19536-j-m-rosen-cheesecake-recall-small-rubber-object-found-in · Updated October 7, 2026 · FDA enforcement record: FDA #F-0973-2018

Cite this page

“J.M. Rosen Cheesecake Recall: Small Rubber Object Found in Product.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/19536-j-m-rosen-cheesecake-recall-small-rubber-object-found-in. Based on FDA recall #F-0973-2018 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0973-2018%22&limit=1).

Why it’s dangerous

A small rubber object was found in the cheesecake by a retail store employee. This object could be a choking hazard for young children, especially if it is small enough to be swallowed.

Who’s affected

Anyone who purchased J.M. Rosen's New York Traditional Cheesecake from retail stores. Young children are at higher risk due to the potential choking hazard from the small rubber object.

How to tell if you have this one

Check for J.M. Rosen's New York Traditional Cheesecake in 6-unit boxes of 4/46 oz. The product has UPC 6 93892 99462 7 and product number 56378. This recall covers all units produced that day.

  • Brand
    J.M. Rosen
  • Product
    J.M. Rosen's Cheesecake - New York Traditional; 6 - Unit- 4/46 oz in a case box; Product #56378 UPC 6 93892 99462 7
  • Category
    Food
FDA recall event · 2 products

All 2 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

  • Classification
    Class II
  • Status
    Terminated
  • Distribution
    One distributor in CA and to retail stores in CA, HI, NV.
Recall numberProduct, codes & lotsQuantity
F-0973-2018J.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).; 6 New York B6-22218 / B7-22218 /B8-22218/ B9-22218119 cases
F-0974-2018J.M. Rosen's Cheesecake - Fantasy; 9 - Unit- 64 Slices in a case box; Product #55993 UPC 6 89076 70759 6; INGREDIENTS: Cream Cheese (Pasteurized Milk. and Cream, Cheese Culture, Salt, ( 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, Eggs, unsalted Butter (Cream (Milk)), Sour Cream (Milk. - Enzymes), Cream, milk, Orange and Lemon Rind, NielsonMasseyVanilla), Chocolate layer cake sour cream, Unbleached Flour. Dark brown sugar, Eggs, Water, Butter, Chocolate (Cocoa Bean, Sugar; Soy Lecithin, Pure Vanilla, Soybean Oil, Cocoa Powder, Baking powder, baking soda, Vanilla Extract, Chocolate Mousse (Cream, Water, Powdered Sugar, Cocoa Powder; Gelatin, Mousse Base{Sugar; Cocoa Powder, Dextrose, Gelatin, Salt), Chocolate. Ganache (Cacao Bean, Sugar, Soy lecithin Vanilla), Dark Chocolate Topping (Cocoa Mass, sugar, cocoa butter, Milkfat, Soy Lecithin Natural Vanilla Contains: Eggs, Milk, Wheat; 9 Fantasy B3-22218 and B4-2221830 cases
Based on the official FDA remedy

What to do — step by step

  1. Check Product Details

    Look for the UPC 6 93892 99462 7 and product number 56378 on the box to confirm if your cheesecake is affected.

Where it went and when

Where it was distributed

Distributed in 3 states.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: not listedILWisconsin: not listedWIMichigan: not listedMINew York: not listedNYRhode Island: not listedRIMassachusetts: not listedMAOregon: not listedORNevada: yesNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: not listedPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: yesCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: not listedVAMaryland: not listedMDDelaware: not listedDEArizona: not listedAZNew Mexico: not listedNMKansas: not listedKSArkansas: not listedARTennessee: not listedTNNorth Carolina: not listedNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: not listedGAHawaii: yesHITexas: not listedTXFlorida: not listedFL

FDA distribution: “One distributor in CA and to retail stores in CA, HI, NV.” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: California, Hawaii, Nevada.

Recall timeline

FDA terminated this recall 13 days after the firm started it.

1. Firm started the recall: Mar 16, 201812. FDA classified it Class II: Mar 27, 201823. FDA terminated the recall: Mar 29, 201834. Published in FDA’s Enforcement Report: Apr 4, 201842018
  1. Firm started the recall
  2. FDA classified it Class II
  3. FDA terminated the recall
  4. Published in FDA’s Enforcement Report

Dates from the agency record only; steps without a date are left out.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #F-0973-2018 (March 16, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0973-2018 to see it in context.
  • Plain-language summary written by qwen3:4b on October 7, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA