Legumbres El Peregrino 16 SL
FDA import alert and refusal historyLa Baneza, SpainFEI 3012423168
Recorded by FDA as LEGUMBRES EL PEREGRINO 16 SL
As of October 26, 2026, Legumbres El Peregrino 16 SL is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on March 17, 2022, most often for required label information not in english (NO ENGLISH).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Beans, corn, and pea, n.e.c. (vegetable) · NO ENGLISH
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Legumbres El Peregrino 16 SL
1 record, newest first. Each line links to the FDA page it came from.
2022
- Import refusalRefused, Beans, corn, and pea, n.e.c. (vegetable)NO ENGLISHEntry 9H5-0006354-4Source
Refusal charges, in plain English
- NO ENGLISH1 refused line
Required label information not in English
Information that must appear on the label appeared not to be given in English, or not to be repeated in every language used on the label.
Questions about Legumbres El Peregrino 16 SL
- Is Legumbres El Peregrino 16 SL on an FDA import alert?
- No listing for Legumbres El Peregrino 16 SL appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Spain page.
- Has FDA refused shipments from Legumbres El Peregrino 16 SL?
- Yes. FDA refused 1 shipment line from Legumbres El Peregrino 16 SL on March 17, 2022. The most recent, on March 17, 2022, was beans, corn, and pea, n.e.c. (vegetable), charged as NO ENGLISH (required label information not in english).
- Why did FDA refuse Legumbres El Peregrino 16 SL's shipments?
- The most frequent charge is NO ENGLISH (required label information not in english, 1 line).
- What is Legumbres El Peregrino 16 SL's FEI number?
- Legumbres El Peregrino 16 SL's FDA Establishment Identifier (FEI) is 3012423168.
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SupplierRadar is not affiliated with the U.S. Food and Drug Administration. Data comes from public FDA records and may contain errors. This is not legal advice; importers remain responsible for their supplier evaluations.