FDA Recall United States Terminated Historical recordClass I
Calico Cottage Inc
- Product
- 1. SALTED NUT ROLL PRE-MADE FUDGE (6SS) 6LB NET WT - not con…
- Published
- June 29, 2022
- Distribution
- Nationwide
Calico Cottage Inc Recall: Fudge contains peanut butter that is potentially contaminated with Salmonella.
United States
TerminatedClass I
- Company
- Calico Cottage Inc
- Product
- 1. PEANUT BUTTER CHOC (3 - 6LB SLABS/CS) 18LB NET WT - Not c…
- Recall date
- May 24, 2022
- Terminated
- October 27, 2022
- Source
- FDA
Reason for recall
Fudge contains peanut butter that is potentially contaminated with Salmonella.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| 1. PEANUT BUTTER CHOC (3 - 6LB SLABS/CS) 18LB NET WT - Not consumer packaging, bulk carton 2. PEANUT BUTTER CHOC FUDGE LAYERED (6S) 6LB NET WT - not consumer packaging, bulk carton 3. PEANUT BUTTER CHOCOLATE FUDGE (6SS) 6LB NET WT - not consumer packaging, bulk carton | Not published in this source record | 677 units total | 1. GTIN: 00673305110936 LOT: 22069041, 22104149, 22118292 2. GTIN: 00673305039084 LOT: 22103099, 22130389 3. GTIN: 00673305039091 LOT: 22074033, 22089039, 22101075, 22103102, 22111217, 22136439, 22137455, 22139488 |
Distribution
- Nationwide
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-1337-2022
- Event ID
- 90345
- Status
- Terminated
- Classification
- Class I
- Company
- Calico Cottage Inc
- Product description
- 1. PEANUT BUTTER CHOC (3 - 6LB SLABS/CS) 18LB NET WT - Not consumer packaging, bulk carton 2. PEANUT BUTTER CHOC FUDGE LAYERED (6S) 6LB NET WT - not consumer packaging, bulk carton 3. PEANUT BUTTER CHOCOLATE FUDGE (6SS) 6LB NET WT - not consumer packaging, bulk carton
- Quantity
- 677 units total
- Reason
- Fudge contains peanut butter that is potentially contaminated with Salmonella.
- Recall initiation date
- May 24, 2022
- Report date
- June 29, 2022
- Classification date
- Not published in this source record
- Termination date
- October 27, 2022
- Distribution pattern
- Nationwide
- UPC, lot, and code information
- 1. GTIN: 00673305110936 LOT: 22069041, 22104149, 22118292 2. GTIN: 00673305039084 LOT: 22103099, 22130389 3. GTIN: 00673305039091 LOT: 22074033, 22089039, 22101075, 22103102, 22111217, 22136439, 22137455, 22139488
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- 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 90345 with 3 other product entries in Public Health Trace.
FDA Recall United States Terminated Historical recordClass I
Calico Cottage Inc
- Product
- 1. PEANUTTIEST CARAMEL CHOCOLATE P-MADE(6SS)6LB NT WT - not…
- Published
- June 29, 2022
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass I
Calico Cottage Inc
- Product
- 1. PEANUT BUTTER FUDGE (3 - 6LB SLABS/CS) 18LB NET WT - not…
- Published
- June 29, 2022
- Distribution
- Nationwide
Responsible company: Calico Cottage Inc
Other recalls from Calico Cottage Inc
FDA Recall United States Terminated Historical recordClass I
Calico Cottage Inc
- Product
- 1. SALTED NUT ROLL PRE-MADE FUDGE (6SS) 6LB NET WT - not con…
- Published
- June 29, 2022
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass I
Calico Cottage Inc
- Product
- 1. PEANUTTIEST CARAMEL CHOCOLATE P-MADE(6SS)6LB NT WT - not…
- Published
- June 29, 2022
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass I
Calico Cottage Inc
- Product
- 1. PEANUT BUTTER FUDGE (3 - 6LB SLABS/CS) 18LB NET WT - not…
- Published
- June 29, 2022
- Distribution
- Nationwide
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 I mean?
A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.
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.
