WESTCO 3065 GOLDEN BAVARIAN CREME FILLING ARTIFICIALLY FLAVORED Ingredients: Water, Sugar, Modified Food Starch, Contain
Summary
The FDA issued a Class II for WESTCO 3065 GOLDEN BAVARIAN CREME FILLING ARTIFICIALLY FLAVORED Ingredients: Wat by BakeMark USA LLC.. Reason: Scheduled process deviation: Final pH of 4.61, 4.66, 4.69, 4.67..
Details
Source
Food Recall
External ID
F-0456-2025
Action Date
2025-02-05
Status
Completed
Category
food
Product Description
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
Lot/Code Info: Item Code 30605 Lot # 62600544 01, 62600544 02, 62600544 03, 62600544 04 USE BY MARCH 16 2025
Quantity Affected: 731 pails (38 lbs)
Reason for Recall
Scheduled process deviation: Final pH of 4.61, 4.66, 4.69, 4.67.
Distribution
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.
Type: Voluntary: Firm initiated
Recall Initiated: 2024-12-03
Company
Pico Rivera, CA
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 47 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (BakeMark USA LLC.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does BakeMark USA LLC. have FDA actions?
This is the only FDA action we have on record for BakeMark USA LLC. in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0456-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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