Recall record at a glance
| Official record | F-2376-2017 |
|---|---|
| Category | Food Recalls |
| Classification | Class I |
| FDA record status | Terminated |
| Recalling firm | L.A. Lucky Import & Export |
| Report date | Jun 21, 2017 |
| Recall initiation date | May 19, 2017 |
| Quantity | 100 cartons (100 BAGS X 2.1 OZ (60 GRAM) = CASE ) |
| Location | Bell, CA, United States |
Official product description
L.A. LUCKY BRAND SWEET BASIL SEEDS: Hot E 2.1 OZ (60 G) BAGS; 100 BAGS PER CASE; Product of Vietnam. Ingredients: Sweet Basil Seeds Serving Size 1.05 oz. (2 servings per container) Distributed by L.A. Lucky Import & Export, Inc., Bell, CA 90201
Why the product was recalled
During follow-up investigation of imported Basil Seeds that were refused for the presence of Salmonella, it was discovered that 100 out of 300 cartons had been distributed.
Distribution information
CA, MI, NE, AZ, MO, UT, IA, FL, CO, WA, TX,, NE, KS, IL, FL, AL, IA
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.