Multigrain Sourdough Freshly Backed, and Half Multigrain Sourdough Artisan Bread, 15 oz; 7 oz, Bag, 1 unit
Summary
The FDA issued a Class II for Multigrain Sourdough Freshly Backed, and Half Multigrain Sourdough Artisan Bread by Giant Eagle, Inc.. Reason: Firm is recalling product due to the potential of foreign material (glass).
Details
Source
Food Recall
External ID
F-0745-2025
Action Date
2025-05-07
Status
Terminated
Category
food
Product Description
Multigrain Sourdough Freshly Backed, and Half Multigrain Sourdough Artisan Bread, 15 oz; 7 oz, Bag, 1 unit
Lot/Code Info: 22765200000 MULTIGRAIN SOURDOUGH FRESHLY BAKED 21762500000 HALF MULTIGRAIN SOURDOUGH ARTISAN BREAD
Quantity Affected: 240 cases
Reason for Recall
Firm is recalling product due to the potential of foreign material (glass)
Distribution
The recalled product was distributed to the following states: PA, OH, MD, IN, WV
Type: Voluntary: Firm initiated
Recall Initiated: 2025-04-12
Company
Pittsburgh, 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 34 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Giant Eagle, Inc. 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 (Giant Eagle, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Giant Eagle, Inc. have FDA actions?
Giant Eagle, Inc. 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-0745-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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