Class IICompletedVoluntary: Firm initiated
BakeMark USA LLC.: food recall F-0456-2025
BakeMark USA LLC. of Pico Rivera, CA recalled WESTCO 3065 GOLDEN BAVARIAN CREME FILLING ARTIFICIALLY FLAVORED Ingredients: Water, Sugar, Modified Food Starch,… Reason: Scheduled process deviation: Final pH of 4.61, 4.66, 4.69, 4.67. The FDA listed it as Class II in its Enforcement Report dated Feb 5, 2025; distribution: 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.
Record status as published: Completed. openFDA data last updated Oct 21, 2026.
Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.
Recall details
- Product
- 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
- Product quantity
- 731 pails (38 lbs)
- Reason for recall
- Scheduled process deviation: Final pH of 4.61, 4.66, 4.69, 4.67.
- Codes, lots and dates on the package
- Item Code 30605 Lot # 62600544 01, 62600544 02, 62600544 03, 62600544 04 USE BY MARCH 16 2025
- Distribution pattern
- 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.
- Recalling firm
- BakeMark USA LLC., Pico Rivera, CA
- Classification
- Class II — the FDA uses this class for a situation in which using or being exposed to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
- Voluntary or mandated
- Voluntary: Firm initiated
- How the firm first notified customers
- Telephone
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Dates
| Event | Date |
|---|---|
| Recall initiated by the firm | Dec 3, 2024 |
| Classified by the FDA | Jan 30, 2025 |
| Published in the Enforcement Report | Feb 5, 2025 |
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Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number F-0456-2025 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
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