Ummp LLC
FDA import alert and refusal historyUlaanbaartar, MongoliaFEI 3012786631
Recorded by FDA as UMMP LLC
As of October 26, 2026, Ummp LLC (Ulaanbaartar, Mongolia) is on the red list of FDA Import Alert 71-04 (Animal food: Salmonella) for dry goat horn (pet chews), published by FDA on April 4, 2025, and has 2 FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 71-04 · red list
- Last import refusal
- Pet chews (non-nutritive), n.e.c. · SALMONELLA
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Ummp LLC
3 records, newest first. Each line links to the FDA page it came from.
2026
- Import refusalRefused, Pet chews (non-nutritive), n.e.c.SALMONELLAEntry 791-5573457-2Source
2025
- Import alert listingListed on Import Alert 71-04red listDRY GOAT HORN (pet chews)Source
- Import refusalRefused, Pet chews (non-nutritive), n.e.c.SALMONELLAEntry 517-0647136-7Source
Refusal charges, in plain English
- SALMONELLA2 refused lines
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 Ummp LLC
- Is Ummp LLC on an FDA import alert?
- Yes. As of October 26, 2026, Ummp LLC is on the red list of FDA Import Alert 71-04, “Animal food: Salmonella”, for dry goat horn (pet chews); FDA published the listing on April 4, 2025.
- Has FDA refused shipments from Ummp LLC?
- Yes. FDA refused 2 shipment lines from Ummp LLC between February 14, 2025 and February 6, 2026. The most recent, on February 6, 2026, was pet chews (non-nutritive), n.e.c., charged as SALMONELLA (salmonella).
- Why did FDA refuse Ummp LLC's shipments?
- The most frequent charge is SALMONELLA (salmonella, 2 lines).
- What is Ummp LLC's FEI number?
- Ummp LLC's FDA Establishment Identifier (FEI) is 3012786631.
- Can shipments from Ummp LLC still enter the U.S.?
- Shipments of dry goat horn (pet chews) from Ummp LLC can be detained without physical examination under Import Alert 71-04; 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.