Recall record at a glance
| Official record | F-0856-2022 |
|---|---|
| Category | Food Recalls |
| Classification | Class II |
| FDA record status | Terminated |
| Recalling firm | El Super Leon Ponchin Snacks, Inc. |
| Report date | Mar 16, 2022 |
| Recall initiation date | Feb 2, 2022 |
| Quantity | 4134 cases of 144 units (total) |
| Location | San Diego, CA, United States |
Official product description
El Super Leon brand, Dry Salted Plum with Chili, Shelf Stable, packaged in plastic bag, Net Wt 1.05oz, UPC 8-52605-00408. With 12 packs of 12 units per case, for a total of 144 units per case. El Leoncito brand, Dry Salted Plum with Chili, Shelf Stable, packaged in plastic bag, Net Wt 1.05oz, UPC 8-52605-00024. The label is read in parts: "Manufactured by: El Super Leon Ponchin Snacks, Inc. 2545 Britannia Blvd. San Diego, CA 92154***PRODUCT OF CHINA***".
Why the product was recalled
Potential to be contaminated with lead.
Distribution information
distributed in CA, AZ, IL, TX, GA, NV.
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: 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.