FDA recall record

Heartland Products Net WT 50 lbs recall — FDA F-0710-2016

Heartland Products Inc., has initiated a recall due to potential contamination with Salmonella involving Milled Flax.

Class Iclassification
F-0710-2016official record ID
Mar 9, 2016report date

Recall record at a glance

Official recordF-0710-2016
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmHeartland Products, Inc.
Report dateMar 9, 2016
Recall initiation dateJan 14, 2016
Quantity43,950 lbs
LocationValley City, ND, United States

Official product description

Heartland Flax 14 Mesh Brown RCM Flax Certified Organic, Net WT 50 lbs. Product packaged in 50 lb Food Grade Plastic bags.

Why the product was recalled

Heartland Products Inc., has initiated a recall due to potential contamination with Salmonella involving Milled Flax.

Distribution information

US: ND, WA, CA, RI, SD, IL. OUS: CANADA

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

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Heartland Products Inc recall — FDA F-1077-2016

Presence of high levels of Azodicarbonamide (ADA), failure to declare allergens on label, and potential cross-contamination with allergens.

Class IIIFDA: TerminatedHeartland Products Inc.