Wegmans brand Mini Muffins; Blueberry; NET WT 20 OZ (1 LB 4 OZ) 567 g; FAMILY PACK; packaged in plastic clamshell; UPC 7
Summary
The FDA issued a Class II for Wegmans brand Mini Muffins; Blueberry; NET WT 20 OZ (1 LB 4 OZ) 567 g; FAMILY PA by Wegmans Food Markets, Inc.. Reason: Product may contain foreign objects of metal origin..
Details
Source
Food Recall
External ID
H-0218-2025
Action Date
2025-07-16
Status
Terminated
Category
food
Product Description
Wegmans brand Mini Muffins; Blueberry; NET WT 20 OZ (1 LB 4 OZ) 567 g; FAMILY PACK; packaged in plastic clamshell; UPC 7789053227
Lot/Code Info: Best by 6/20 W
Quantity Affected: 8508 units total
Reason for Recall
Product may contain foreign objects of metal origin.
Distribution
NY, PA, MA, NJ, MD, VA, DC, NC, DE
Type: Voluntary: Firm initiated
Recall Initiated: 2025-06-14
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 147 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 "H-0218-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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