Culinaria Branded Roasted & Salted Colossal Cashew & Macadamia Mix. Net Wt 9oz (255g) UPC 0 41318-22428 3. Distributed
Summary
The FDA issued a Class II for Culinaria Branded Roasted & Salted Colossal Cashew & Macadamia Mix. Net Wt 9oz by A. L. Schutzman Company, Inc.. Reason: Label mix-up..
Details
Source
Food Recall
External ID
F-0952-2023
Action Date
2023-05-31
Status
Completed
Category
food
Product Description
Culinaria Branded Roasted & Salted Colossal Cashew & Macadamia Mix. Net Wt 9oz (255g) UPC 0 41318-22428 3. Distributed by Schnuck Markets, Inc., St. Louis, MO 63146-6928.
Lot/Code Info: Code is ink jet printed on bottom of can. Lot 3033A9 Best By 2/2/2025
Quantity Affected: 828 cans
Reason for Recall
Label mix-up.
Distribution
IL, IN, MO
Type: Voluntary: Firm initiated
Recall Initiated: 2023-04-26
Company
Waukesha, WI
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 71 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 (A. L. Schutzman Company, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does A. L. Schutzman Company, Inc. have FDA actions?
This is the only FDA action we have on record for A. L. Schutzman Company, Inc. in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0952-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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