Recall record at a glance
| Official record | F-1536-2020 |
|---|---|
| Category | Food Recalls |
| Classification | Class II |
| FDA record status | Ongoing |
| Recalling firm | Freshouse Produce |
| Report date | Sep 30, 2020 |
| Recall initiation date | Aug 7, 2020 |
| Quantity | 2,870 mesh bags + 40/40lb boxes |
| Location | Salisbury, NC, United States |
Official product description
Freshouse Limes, 2lb mesh bag, UPC 33383 14683 & Nature Promise Organic Limes, 1lb mesh bag, UPC 88267 53813
Why the product was recalled
The firm received positive Environmental sampling results for Listeria monocytogenes.
Distribution information
Product was shipped to the following states: MD, NC, PA, SC, & VA. North Carolina, Pennsylvania, South Carolina, and Virginia and to wholesalers in Maryland
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: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.
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.