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J.M.Rosen Cheesecake Recall: Retail store employee noticed a small rubber object in the cheesecake - the firm is recalling the entire day's production.

United States

TerminatedClass II

Company
J.M.Rosen Cheesecake
Product
J.M. Rosen's Cheesecake - New York Traditional; 6 - Unit-…
Recall date
March 16, 2018
Terminated
March 29, 2018
Source
FDA

Reason for recall

Retail store employee noticed a small rubber object in the cheesecake - the firm is recalling the entire day's production.

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
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). Not published in this source record 119 cases 6 New York B6-22218 / B7-22218 /B8-22218/ B9-22218

Distribution

  • One distributor in CA and to retail stores in CA
  • HI
  • NV.

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-0973-2018
Event ID
79578
Status
Terminated
Classification
Class II
Company
J.M.Rosen Cheesecake
Product description
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
Reason
Retail store employee noticed a small rubber object in the cheesecake - the firm is recalling the entire day's production.
Recall initiation date
March 16, 2018
Report date
April 4, 2018
Classification date
Not published in this source record
Termination date
March 29, 2018
Distribution pattern
One distributor in CA and to retail stores in CA, HI, NV.
UPC, lot, and code information
6 New York B6-22218 / B7-22218 /B8-22218/ B9-22218
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
Letter
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Other products recalled under this same event

This recall shares FDA event ID 79578 with 1 other product entry in Public Health Trace.

FDA Recall United States Terminated Historical recordClass II

J.M.Rosen Cheesecake

Product
J.M. Rosen's Cheesecake - Fantasy; 9 - Unit- 64 Slices in…
Published
April 4, 2018
Distribution
One distributor in CA and to retail stor…

View recall →

Responsible company: J.M.Rosen Cheesecake

Other recalls from J.M.Rosen Cheesecake

FDA Recall United States Terminated Historical recordClass II

J.M.Rosen Cheesecake

Product
J.M. Rosen's Cheesecake - Fantasy; 9 - Unit- 64 Slices in…
Published
April 4, 2018
Distribution
One distributor in CA and to retail stor…

View recall →

Distribution map

A map highlighting the states named in the source's distribution description.

Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.

Distribution map
State Distributed
California 1
Hawaii 1
Nevada 1

States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace:

Frequently asked questions

What does a Class II mean?

A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

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This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.