RecallHawk
Class II Recall

WESTCO 3065 GOLDEN BAVARIAN CREME FILLING ARTIFICIALLY FLAVORED Ingredients: Water, Sugar, Modified Food Starch, Contain

BakeMark USA LLC.

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

BakeMark USA LLC.

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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