Recall record at a glance
| Official record | F-1571-2015 |
|---|---|
| Category | Food Recalls |
| Classification | Class I |
| FDA record status | Terminated |
| Recalling firm | Henrys Farm Inc. |
| Report date | Apr 1, 2015 |
| Recall initiation date | Jan 22, 2015 |
| Location | Woodford, VA, United States |
Official product description
1lb mungbean sprouts 15 box (20 bags a box) a week. 10lb mungbean sprouts 30 bag a week. These products are labeled as produced by Henrys Farm Inc
Why the product was recalled
Listeria contamination was discovered at Henry's Farm, Inc., a grower and manufacturer of soybean sprouts, after sampling by the US Food and Drug Administration. Sample 875780 . Henrys Farm Inc. of Woodford, VA is recalling all packages of Soybean Sprouts because they may be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections to indiv
Distribution information
Maryland and Virginia to three Consignees
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: Letter.
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.