Wegmans single serve snack tray (5.7oz) packaged in a clear square plastic packaging with fruit, almonds and cheese 6 t
Summary
The FDA issued a Class II for Wegmans single serve snack tray (5.7oz) packaged in a clear square plastic pack by Stellex/CF Houston, LLC. Reason: Undeclared almonds and/or undeclared wheat.
Details
Source
Food Recall
External ID
F-1225-2023
Action Date
2023-07-12
Status
Terminated
Category
food
Product Description
Wegmans single serve snack tray (5.7oz) packaged in a clear square plastic packaging with fruit, almonds and cheese 6 trays per case
Lot/Code Info: Best By 05/23/2023 Lot Code 005OFH2301
Quantity Affected: 321 cases
Reason for Recall
Undeclared almonds and/or undeclared wheat
Distribution
Distributed to a single distribution center, located in PA, who then delivers to cross docks, located in NY, to be delivered to retail locations.
Type: Voluntary: Firm initiated
Recall Initiated: 2023-06-15
Company
Houston, TX
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 228 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Stellex/CF Houston, LLC has 7 FDA actions in our database, including 7 recalls.
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 (Stellex/CF Houston, LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Stellex/CF Houston, LLC have FDA actions?
Stellex/CF Houston, LLC has 7 FDA actions in our database, including 7 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1225-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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