Wegmans Penne Rigate Mozzarella Salad Net Wt 30 OZ (1 LB 14 OZ) 850 g. Packaged in a plastic container.
Summary
The FDA issued a Class II for Wegmans Penne Rigate Mozzarella Salad Net Wt 30 OZ (1 LB 14 OZ) 850 g. Packaged by ASK Foods Inc. Reason: Undeclared milk allergen.
Details
Source
Food Recall
External ID
F-0998-2023
Action Date
2023-06-28
Status
Terminated
Category
food
Product Description
Wegmans Penne Rigate Mozzarella Salad Net Wt 30 OZ (1 LB 14 OZ) 850 g. Packaged in a plastic container.
Lot/Code Info: 3515-2 and USE BY 06/1/23
Quantity Affected: 600 units
Reason for Recall
Undeclared milk allergen
Distribution
Distributed to a distribution center in NY and then further distributed to stores in New York, Pennsylvania, and Massachusetts.
Type: Voluntary: Firm initiated
Recall Initiated: 2023-05-25
Company
Palmyra, PA
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 17 food recalls issued in the same week, part of 204 food-related FDA actions this month.
ASK Foods Inc has 2 FDA actions in our database, including 2 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 (ASK Foods Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does ASK Foods Inc have FDA actions?
ASK Foods Inc has 2 FDA actions in our database, including 2 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0998-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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