FDA Recall United States Terminated Historical recordClass II
Coborn's, Inc
- Product
- Coborn's/Cash Wise American Rye Bread - UPC 7-33147-20150 N…
- Published
- October 11, 2017
- Distribution
- Coborn's, Marketplace, and Cashwise stor…
Coborn's, Inc Recall: While reviewing the allergen listings for our products and cross referencing against the updated spec sheet from the manufacturer of the bread base, it was discovered that the allergen statement had been updated from only wheat to wheat, milk, egg and soy.
United States
TerminatedClass II
- Company
- Coborn's, Inc
- Product
- Coborn's/Cash Wise Caraway Rye Bread - UPC 7-33147-20155-8…
- Recall date
- September 6, 2017
- Terminated
- August 15, 2019
- Source
- FDA
Reason for recall
While reviewing the allergen listings for our products and cross referencing against the updated spec sheet from the manufacturer of the bread base, it was discovered that the allergen statement had been updated from only wheat to wheat, milk, egg and soy.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Coborn's/Cash Wise Caraway Rye Bread - UPC 7-33147-20155-8 Net Wt. 16 oz (1.0 lb) (454 g) Sell by 9/6/2017 | 7-33147-20155-8 | 121 loaves (total) | Sell by 9/7/2017 |
Distribution
- Coborn's
- Marketplace
- and Cashwise stores in MN
- WI
- ND
- and SD.
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-3611-2017
- Event ID
- 78089
- Status
- Terminated
- Classification
- Class II
- Company
- Coborn's, Inc
- Product description
- Coborn's/Cash Wise Caraway Rye Bread - UPC 7-33147-20155-8 Net Wt. 16 oz (1.0 lb) (454 g) Sell by 9/6/2017
- Quantity
- 121 loaves (total)
- Reason
- While reviewing the allergen listings for our products and cross referencing against the updated spec sheet from the manufacturer of the bread base, it was discovered that the allergen statement had been updated from only wheat to wheat, milk, egg and soy.
- Recall initiation date
- September 6, 2017
- Report date
- October 11, 2017
- Classification date
- Not published in this source record
- Termination date
- August 15, 2019
- Distribution pattern
- Coborn's, Marketplace, and Cashwise stores in MN, WI, ND, and SD.
- UPC, lot, and code information
- UPC 7-33147-20155-8; Sell by 9/7/2017
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Other products recalled under this same event
This recall shares FDA event ID 78089 with 1 other product entry in Public Health Trace.
Responsible company: Coborn's, Inc
Other recalls from Coborn's, Inc
FDA Recall United States Terminated Historical recordClass I
Coborn's, Inc
- Product
- Chicken Salad Sandwich, UPC 2 07209-XXXXX. Keep Refrigerate…
- Published
- October 30, 2019
- Distribution
- Multiple states
FDA Recall United States Terminated Historical recordClass I
Coborn's, Inc
- Product
- Chicken Salad Croissant Sandwich, UPC 2 07275-XXXXX. Keep R…
- Published
- October 30, 2019
- Distribution
- Multiple states
FDA Recall United States Terminated Historical recordClass I
Coborn's, Inc
- Product
- Chicken Salad on Marble Rye, UPC 2 05118-XXXXX. Keep Refrig…
- Published
- October 30, 2019
- Distribution
- Multiple states
A map highlighting the states named in the source's distribution description.
Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.
| State | Distributed |
|---|---|
| Minnesota | 1 |
| Wisconsin | 1 |
| North Dakota | 1 |
| South Dakota | 1 |
States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.
Where this information comes from
View FDA enforcement record -- the specific openFDA record this summary was built from.
No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
Technical source data
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
Frequently asked questions
What does a Class II mean?
A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.
Is this recall still active?
According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
What should I do if I have this product?
Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.
Where can I find more official information?
The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.
This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.
