Barnies
FDA import alert and refusal historyAjax, CanadaFEI 3009324964
As of October 25, 2026, Barnies (Ajax, Canada) is on the red list of FDA Import Alert 71-04 (Animal food: Salmonella) for dried beef lung treats, published by FDA on March 31, 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 dog food n.e.c. · SALMONELLA
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Barnies
3 records, newest first. Each line links to the FDA page it came from.
2025
- Import alert listingListed on Import Alert 71-04red listDried Beef Lung TreatsSource
2017
- Import refusalRefused, Pet dog food n.e.c.SALMONELLAEntry 799-0741443-4Source
- Import refusalRefused, Pet dog food n.e.c.SALMONELLAEntry 799-9336725-4Source
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 Barnies
- Is Barnies on an FDA import alert?
- Yes. As of October 25, 2026, Barnies is on the red list of FDA Import Alert 71-04, “Animal food: Salmonella”, for dried beef lung treats; FDA published the listing on March 31, 2025.
- Has FDA refused shipments from Barnies?
- Yes. FDA refused 2 shipment lines from Barnies between March 16, 2017 and June 15, 2017. The most recent, on June 15, 2017, was pet dog food n.e.c., charged as SALMONELLA (salmonella).
- Why did FDA refuse Barnies's shipments?
- The most frequent charge is SALMONELLA (salmonella, 2 lines).
- What is Barnies's FEI number?
- Barnies's FDA Establishment Identifier (FEI) is 3009324964.
- Can shipments from Barnies still enter the U.S.?
- Shipments of dried beef lung treats from Barnies 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.