WESTCO 3065 GOLDEN BAVARIAN CREME FILLING ARTIFICIALLY FLAVORED Ingredients recall
Recalled by BakeMark USA LLC. · Pico Rivera, CA, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Scheduled process deviation: Final pH of 4.61, 4.66, 4.69, 4.67.
These are failures of the safety steps that keep food safe - cooking, pasteurising, keeping cold, sealing - even when no contaminant has yet been found. All processing & sanitation problems recalls.
What was recalled
WESTCO 3065 GOLDEN BAVARIAN CREME FILLING ARTIFICIALLY FLAVORED Ingredients: Water, Sugar, Modified Food Starch, Contains 2% or Less of: Artificial Flavor, Salt, Color (Titanium Dioxide, Yellow 5, Yellow 6), Preservatives (Sodium Benzoate, Sorbic Acid, Potassium Sorbate, Phosphoric Acid, Citric Acid. NET WEIGHT: 38 LB (17.3 KG) DISTRIBUTED BY BAKEMARK PICO RIVERA, CA 90660 USA 00018609306058 62600544
Quantity: 731 pails (38 lbs)
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.
Item Code 30605 Lot # 62600544 01, 62600544 02, 62600544 03, 62600544 04 USE BY MARCH 16 2025
Where it was sold
Alabama Florida Georgia Iowa Illinois Indiana Kentucky Louisiana Michigan Minnesota Mississippi North Dakota New Jersey New York Ohio Pennsylvania South Carolina South Dakota Tennessee Texas Wisconsin West Virginia
FDA's distribution note: Product was shipped to the following states: AL, FL, GA, IA, IL, IN, KY, LA, MI, MN, MS, ND, NJ, NY, OH, PA, SC, SD, TN, TX, WI & WV.
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 completed: 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
- BakeMark USA LLC.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Dec 3, 2024
- In FDA report of
- Feb 5, 2025
- FDA recall number
- F-0456-2025 · event 95894
- Official record
- FDA enforcement report search