Somerdale Red Dragon Cheddar Cheese, cut and repacked in plastic cheese wrap by Wegmans and sold by the pound.
Summary
The FDA issued a Class II for Somerdale Red Dragon Cheddar Cheese, cut and repacked in plastic cheese wrap by by Wegmans Food Markets, Inc.. Reason: Cheese label does not declare wheat from ale wash.
Details
Source
Food Recall
External ID
F-0766-2021
Action Date
2021-07-07
Status
Terminated
Category
food
Product Description
Somerdale Red Dragon Cheddar Cheese, cut and repacked in plastic cheese wrap by Wegmans and sold by the pound.
Lot/Code Info: All product packed on April 23, 2021, or later
Quantity Affected: 1299 lbs.
Reason for Recall
Cheese label does not declare wheat from ale wash
Distribution
Maryland, Massachusetts, New Jersey, New York, North Carolina, Pennsylvania, Virginia
Type: Voluntary: Firm initiated
Recall Initiated: 2021-06-14
Company
Rochester, NY
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.
Wegmans Food Markets, Inc. has 28 FDA actions in our database, including 28 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 (Wegmans Food Markets, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Wegmans Food Markets, Inc. have FDA actions?
Wegmans Food Markets, Inc. has 28 FDA actions in our database, including 28 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0766-2021" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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