Multigrain Sourdough Freshly Backed, and Half Multigrain Sourdough Artisan Bread, 15 oz…
Giant Eagle, Inc. recalled this product and the FDA reported the enforcement action on 7 May 2025 as Class II. The recall was initiated by the firm. Firm is recalling product due to the potential of foreign material (glass)
The record
Every field below is published by the FDA in the openFDA food enforcement database. Check the FDA notice before acting on any recall: this page is a reading of the public record, not a substitute for it.
- Product
- Multigrain Sourdough Freshly Backed, and Half Multigrain Sourdough Artisan Bread, 15 oz; 7 oz, Bag, 1 unit
- Reason for recall
- Firm is recalling product due to the potential of foreign material (glass)
- Recalling firm
- Giant Eagle, Inc.
- Firm location
- Pittsburgh, Pennsylvania, United States
- Classification
- Class II
- Status
- Terminated
- Recall number
- F-0745-2025
- Quantity
- 240 cases
- Distribution
- The recalled product was distributed to the following states: PA, OH, MD, IN, WV
- Initiated
- 12 April 2025
- Reported by FDA
- 7 May 2025
- Terminated
- 2 May 2025
- Firm notified by
- Product codes
- 22765200000 MULTIGRAIN SOURDOUGH FRESHLY BAKED 21762500000 HALF MULTIGRAIN SOURDOUGH ARTISAN BREAD
Reading this record
Five things about this record are not in the record itself, and each one changes how it should be read.
- Class II means the FDA judged a remote probability of serious harm, or a probability of temporary or medically reversible harm. The class is assigned by an agency health hazard evaluation under 21 CFR 7.41, not by the firm.
- The firm started this recall itself. Most FDA food recalls are voluntary, and a recall is a food safety plan working rather than failing. The circumstances in which the agency asks for one instead are set out in 21 CFR 7.45.
- This record is the only one the FDA opened for its recall event, so it covers a single product code.
- The recall ran for 3 weeks, from 12 April 2025 to termination on 2 May 2025. Termination means the agency judged that all reasonable effort had been made, under 21 CFR 7.55, and it says nothing about whether product remained in circulation.
- The distribution pattern names 4 states, and the FDA published the enforcement report 4 weeks after the firm began the recall.
- Recalls of a bakery product run a median of 6 months, so this one was shorter than usual for its category. Bakery is overwhelmingly an allergen category rather than a pathogen one: baking is a kill step, but a bakery runs many recipes down shared lines, so the failure that recalls a bakery product is usually a label or a changeover.
Named in the distribution pattern: Ohio, Maryland, Indiana, West Virginia. Those pages count recalls by where the RECALLING FIRM sits, which is a different question from where this product went.
What this recall was for
Foreign material
A foreign material recall means something that is not food was found in food: metal, plastic, glass, wood or insect matter, usually shed by equipment during processing.
A preventive controls plan covers foreign material under the clauses below. This is where the control belongs, not a finding against any firm named on this page: a recall record states a reason, and most of these recalls were initiated by the firm itself.
- 21 CFR 117.40
- Equipment and utensils: plant equipment designed and maintained so it cannot contaminate food with lubricants, fuel, metal fragments or contaminated water.
- 21 CFR 117.80(c)
- Manufacturing operations: the measures that protect food from contamination during processing, including the effective ones against metal and other extraneous material.
- 21 CFR 117.150
- Corrective actions: what a facility does when a preventive control was not properly implemented, including identifying and correcting the problem and evaluating the food for safety.
Filed under bakery. A product can sit in more than one.
Other bakery recalls for the same reason
These are the closest records in the corpus: the same kind of food, recalled for a hazard this record also names. Unlike the firm’s own records below, they come from different companies, which is what makes them a pattern rather than a history.
Other records from Giant Eagle, Inc.
The FDA opens one enforcement record per product code, so several of these are frequently one recall event. 62 other records name this firm.
| Reported | Product | Firm | Reason | Class |
|---|---|---|---|---|
| 2025-10-29 | Smoked Mozzarella Penne Salad, bulk, UPC 256616000000 | Giant Eagle, Inc. | Recall notification from supplier of Potential listeria contamination. | Class I |
| 2025-10-29 | Smoked Mozzarella Penne Salad-Large, Clam shell and Bowl, 9 lbs, Individual Unit, Keep Refrigerated, UPC 246512000000 | Giant Eagle, Inc. | Recall notification from supplier of Potential listeria contamination. | Class I |
| 2025-10-29 | Smoked Mozzarella Penne Salad-Small, Clam shell and Bowl, 4 lbs 8 oz, Individual Unit, Keep Refrigerated, UPC 246511000000 | Giant Eagle, Inc. | Recall notification from supplier of Potential listeria contamination. | Class I |
| 2022-04-20 | Giant Eagle, Happy Face Cookie 4 Pack 25051900000, 11 oz, Clam Shell | Giant Eagle, Inc. | Undeclared milk allergen | Class I |
| 2022-04-20 | Giant Eagle, Happy Face Cookie Single 25065900000 | Giant Eagle, Inc. | Undeclared milk allergen | Class I |
| 2022-01-05 | Giant Eagle Diced Green Peppers, 10 oz. 283 g, Frozen bag, 12 packages per case , Best By 10/14/2023 . | Giant Eagle, Inc. | Giant Eagle, Inc., Pittsburgh, PA has initiated a recall of Giant Eagle Diced Green Peppers, 10 oz. 283 g, Frozen bag, 12 packages per case, Best By 10/14/2023 because the product tested positive for Listeriosis Monocytogenes. | Class II |
| 2021-06-09 | Giant Eagle Chicken Street Taco Kit; 20 oz (1 lbs 4 oz) Individual Units, PLU Code beginning 256598 00000 | Giant Eagle, Inc. | Undeclared egg allergen | Class I |
| 2017-11-22 | Giant Eagle Breaded Shrimp Pittsburgh, PA 15238 PLU # 86815 refrigerated, packed in plastic clam shell. Sell by dates: up to and including Oct 25 2017. Located in the Grab "n Go refrigerated cases at Giant Eagle and Market District supermarkets. | Giant Eagle, Inc. | Giant Eagle Voluntarily Recalls Breaded Shrimp Due to an Undeclared Egg Allergen. All lot codes up to and including best by October 24, 2017 of Giant Eagle brand Breaded Shrimp, prepared and sold from the Prepared Foods grab and go sections inside Giant Eagle and Market District supermarkets through October 19, 2017 have been voluntarily recalled by Giant Eagle due to an undeclared egg allergen. | Class I |
| 2017-11-15 | Market District Coffee Beans covered in Dark Chocolate; Net Wt. 8 OZ.; Contains Soy; May Contain: Milk Manufactured in a plant that processes wheat, peanuts, tree nuts and eggs.; Distributed by Giant Eagle, Inc., Pittsburgh, PA 15238-2809 | Giant Eagle, Inc. | On 10/30/2017, Giant Eagle received notice from their contract manufacturer to recall Market District Coffee Beans Covered in Dark Chocolate due to undeclared milk in the dark chocolate. Giant Eagle product labels do carry the advisory statement "May Contain Milk". | Class II |
| 2017-11-15 | Market District Powerberry Mix covered in Dark Chocolate; Net Wt. 8 OZ.; Contains Soy; May Contain: Milk Manufactured in a plant that processes wheat, peanuts, tree nuts and eggs.; Distributed by Giant Eagle, Inc., Pittsburgh, PA 15238-2809 | Giant Eagle, Inc. | On 10/30/2017, Giant Eagle received notice from their contract manufacturer, to recall Market District Powerberry Mix Covered in Dark Chocolate, due to undeclared milk in the dark chocolate. Giant Eagle product labels do carry the advisory statement "May Contain Milk". | Class II |
All 63 records for Giant Eagle, Inc.
All 2025 recalls · All FDA food recall data
21 CFR 117.40 is the clause behind this recall, and it is one somebody has to produce evidence for at their next audit. Krolda maps supplier documents to the clause they satisfy in FSSC 22000, IFS Food and 21 CFR 117, and routes the corrective action when the evidence is missing.
Early accessRecall records come from the openFDA food enforcement API, published by the U.S. Food and Drug Administration in the public domain. Krolda adds the hazard classification and the clause mapping; neither is an FDA determination. Always check the FDA notice before acting on a recall.