RecallHawk
Class III Recall

Super Size Golden Harvest Carrot Cate, Item 06233. Net 9.8 kg 345 oz (21 lb 9 oz). UPC 7 70118-06233 6. Keep Frozen.

The Original Cakerie Ltd.

Summary

The FDA issued a Class III for Super Size Golden Harvest Carrot Cate, Item 06233. Net 9.8 kg 345 oz (21 lb 9 by The Original Cakerie Ltd.. Reason: Pieces of cashew and almond were found in box of walnuts which were used to make carrot cake..

Details

Source

Food Recall

External ID

F-0342-2023

Action Date

2023-02-15

Status

Completed

Category

food

Product Description

Super Size Golden Harvest Carrot Cate, Item 06233. Net 9.8 kg 345 oz (21 lb 9 oz). UPC 7 70118-06233 6. Keep Frozen. Manufactured by: The Original Cakerie LTD, 1345 Cliveden Ave, Delta BC Canada V3M 6C7

Lot/Code Info: Lot Code: 32921 Expiration Date: 25 November 2023

Quantity Affected: 384 cases

Reason for Recall

Pieces of cashew and almond were found in box of walnuts which were used to make carrot cake.

Distribution

MN, NC, VA

Type: Voluntary: Firm initiated

Recall Initiated: 2023-01-13

Context & Analysis

This is a Class III recall. Class III recalls involve products unlikely to cause adverse health consequences, but that violate FDA regulations.

This was one of 30 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Frequently Asked Questions

What is a Class III recall?

A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.

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 (The Original Cakerie Ltd.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does The Original Cakerie Ltd. have FDA actions?

This is the only FDA action we have on record for The Original Cakerie Ltd. in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0342-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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