Wishbone SRL
FDA import alert and refusal historyYerba Buena, ArgentinaFEI 3014061010
As of October 25, 2026, Wishbone SRL (Yerba Buena, Argentina) is on the red list of FDA Import Alert 99-19 (Food products: Salmonella) for sesame seed, published by FDA on December 16, 2022, and has 1 FDA import refusal recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 99-19 · red list
- Last import refusal
- Sesame seed (edible seed) · SALMONELLA
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Wishbone SRL
2 records, newest first. Each line links to the FDA page it came from.
2022
- Import alert listingListed on Import Alert 99-19red listSesame SeedSource
- Import refusalRefused, Sesame seed (edible seed)SALMONELLAEntry 83M-0013156-7Source
Refusal charges, in plain English
- SALMONELLA1 refused line
Salmonella
The product appeared to contain Salmonella, which the law treats as a poisonous and deleterious substance that may make food injurious to health.
Questions about Wishbone SRL
- Is Wishbone SRL on an FDA import alert?
- Yes. As of October 25, 2026, Wishbone SRL is on the red list of FDA Import Alert 99-19, “Food products: Salmonella”, for sesame seed; FDA published the listing on December 16, 2022.
- Has FDA refused shipments from Wishbone SRL?
- Yes. FDA refused 1 shipment line from Wishbone SRL on December 13, 2022. The most recent, on December 13, 2022, was sesame seed (edible seed), charged as SALMONELLA (salmonella).
- Why did FDA refuse Wishbone SRL's shipments?
- The most frequent charge is SALMONELLA (salmonella, 1 line).
- What is Wishbone SRL's FEI number?
- Wishbone SRL's FDA Establishment Identifier (FEI) is 3014061010.
- Can shipments from Wishbone SRL still enter the U.S.?
- Shipments of sesame seed from Wishbone SRL can be detained without physical examination under Import Alert 99-19; FDA releases them only if evidence shows they do not have the listed violation. Importers must consider this listing in their FSVP evaluation (21 CFR 1.505).
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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.