FDA recall record

United Natural Trading Inc. dba Woodstock Farms Market Basket Fiber Frenzy 10oz recall — FDA F-3345-2017

The firm's supplier (of dates/apricots) found Listeria monocytogenes within their facility. As a safety precaution, the firm has recalled their products…

Class Iclassification
F-3345-2017official record ID
Aug 9, 2017report date

Recall record at a glance

Official recordF-3345-2017
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmUnited Natural Trading Inc. dba Woodstock Farms
Report dateAug 9, 2017
Recall initiation dateJun 15, 2017
Quantity491 Cases
LocationEdison, NJ, United States

Official product description

Market Basket Fiber Frenzy 10oz.

Why the product was recalled

The firm's supplier (of dates/apricots) found Listeria monocytogenes within their facility. As a safety precaution, the firm has recalled their products that may contain dates/apricots.

Distribution information

The products were shipped to retailers and distributors in limited quantities throughout the United States.

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: 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.