FDA recall record

Del Monte Research Center - Walnut Creek Cut Green Beans packed under brand names of: Allens recall — FDA F-0212-2017

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…

Class Iclassification
F-0212-2017official record ID
Oct 26, 2016report date

Recall record at a glance

Official recordF-0212-2017
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmDel Monte Research Center - Walnut Creek
Report dateOct 26, 2016
Recall initiation dateSep 23, 2016
Quantity15, 859 cases (6 cans per case) total, all varieties
LocationWalnut Creek, CA, United States

Official product description

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

Why the product was recalled

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.

Distribution information

US distribution only to AL, AR, CO, IL, MD, MO, MS, FL, GA, KS, KY, LA, OK, PA, NC, SC, TN, TX, UT, VA, WI, WV.

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.

Related recall records

Other records from the same recalling company are shown first when available.