FDA recall record

Inn Foods IQF Italian Cut Green Beans recall — FDA F-2935-2015

Due to customer request a sample of IQF Italian Cut Green Beans was sent to 3rd party laboratory found to be positive for Listeria monocytogenes.

Class IIclassification
F-2935-2015official record ID
Aug 12, 2015report date

Recall record at a glance

Official recordF-2935-2015
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmInn Foods Inc.
Report dateAug 12, 2015
Recall initiation dateJun 30, 2015
Quantity8 totes
LocationWatsonville, CA, United States

Official product description

IQF Italian Cut Green Beans (each tote 1350 lbs) lot 880804 Harvest Delight Italian Green Beans, (Veg, mixed, FZN, Italian Blend, IQF) 2 lb. poly bags, 12 x 2 lbs, per case Lot 87151056, 960 cases, packed on 4/30/15; Harvest Delight Italian Green Beans, Lot 880271056, 848 cases, packed on 6/9/15; MFG SKU: 10568.

Why the product was recalled

Due to customer request a sample of IQF Italian Cut Green Beans was sent to 3rd party laboratory found to be positive for Listeria monocytogenes.

Distribution information

CA and Republic of Djibouti, Dubai and Italy

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Telephone.

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.