FDA recall record

Mary's Harvest Fresh Foods Vegetable Tray Rectangle, 4/40 oz recall — FDA F-3421-2017

Product is recalled due to potential contamination with E.coli O26.

Class IIclassification
F-3421-2017official record ID
Aug 30, 2017report date

Recall record at a glance

Official recordF-3421-2017
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmMary's Harvest Fresh Foods, Inc.
Report dateAug 30, 2017
Recall initiation dateAug 3, 2017
Quantity12 cases (4/40 oz. packages) and 34 cases (4/18 oz. packages)
LocationPortland, OR, United States

Official product description

Mary's Harvest brand, Vegetable Tray Rectangle, 4/40 oz. packages, UPC 0 9250475701 6. Mary's Harvest brand, Vegetable Tray Rectangle, 4/18 oz packages, UPC 0 9250475712 2. Ingredients: Celery, Grape Tomatoes, Sugar Snap Peas, Broccoli, Carrots, and Ranch Dip.

Why the product was recalled

Product is recalled due to potential contamination with E.coli O26.

Distribution information

distributed in OR and WA

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: E-Mail.

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.