United States
TerminatedClass I
Customer complaint of finding crawfish parts in green beans initiated this recall for approximately 15,000 cases of 106 oz. metal cans of green beans or field peas with snaps sold under various brand names.
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Cut Green Beans packed under brand names of: Allens Cut Green Beans (Ejotes Cortados Lago Azul) Blue Lake . Allens Cracker Barrel Label (Both labels have same UPC # - different sodium content - 140 mg for Allens Cut Green Beans and 250 for Cracker Barrel label Peso Neto: 6 lbs 10 oz. (3.00 kg) UPC 0 34700 01224 7; Distributed by Sager Creek Vegetable Company, Siloam Springs, AR 72761-0250 USA; Monarch Blue Lake Green Beans (De Primera, Lago Azul Ejotes Cortados, Tamano 4); Peso Neto 6 lb. 10 oz. (3 kg) UPC 7 58108 01041 3 Monarch Cut Green Beans mixed Sieve; NET WT. 6 lb. 10 oz. (3.00kg); UPC: 7 58108 01048 2 Distributed by US Foods, Inc. Rosemont, IL 60018; SYSCO Reliance Green Beans (Ejotes), Cut Mix Sieve; NET WT. 6 lb. 10 oz. (300 kg) UPC 0 74865 12172 9 SYSCO Green Beans, Mixed & Short Cuts; NET. WT. 6 lb. 10 oz. (3.00 kg) UPC: 0 74865 12175 0; Distributed by Sysco Corporation, Houston, TX Silver Source Short Cut Green Beans; NET WT. 6 lb. 10 oz. (3.00 kg) UPC 8 06795 02895 9 Distributed by Performance Food Group, Richmond, VA 23238 | Not published in this source record | 15, 859 cases (6 cans per case) total, all varieties | Lot Number 615383 Best By Date 06 01 19 |
This recall shares FDA event ID 75277 with 1 other product entry in Public Health Trace.
FDA Recall United States TerminatedTerminated: May 8, 2017Historical recordClass I
Responsible company: Del Monte Research Center - Walnut Creek
FDA Recall United States TerminatedTerminated: April 17, 2019Historical recordClass II
FDA Recall United States TerminatedTerminated: July 20, 2017Historical recordClass II
FDA Recall United States TerminatedTerminated: May 8, 2017Historical recordClass I
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 |
|---|---|
| Alabama | 1 |
| Arkansas | 1 |
| Colorado | 1 |
| Illinois | 1 |
| Maryland | 1 |
| Missouri | 1 |
| Mississippi | 1 |
| Florida | 1 |
| Georgia | 1 |
| Kansas | 1 |
| Kentucky | 1 |
| Louisiana | 1 |
| Oklahoma | 1 |
| Pennsylvania | 1 |
| North Carolina | 1 |
| South Carolina | 1 |
| Tennessee | 1 |
| Texas | 1 |
| Utah | 1 |
| Virginia | 1 |
| Wisconsin | 1 |
| West Virginia | 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.
View FDA enforcement record -- the specific openFDA record this summary was built from.
This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.
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View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
FDA classifies this recall as Class I. See how to read an FDA recall record (linked above) for what each classification level means.
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.
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This record is preserved as published by FDA, as of May 8, 2017.
Status as reported: Terminated.
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