Dailis Pty Ltd T/a Natural Pet Treats Australia
FDA import alert and refusal historyCaloundra West, AustraliaFEI 3010154895
As of October 27, 2026, Dailis Pty Ltd T/a Natural Pet Treats Australia (Caloundra West, Australia) is on the red list of FDA Import Alert 71-04 (Animal food: Salmonella) for roo bites; green lip mussel; lamb puff ovine lung, published by FDA on April 1, 2025, and has no 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
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Dailis Pty Ltd T/a Natural Pet Treats Australia
1 record, newest first. Each line links to the FDA page it came from.
2025
- Import alert listingListed on Import Alert 71-04red listRoo Bites; Green Lip Mussel; Lamb Puff Ovine LungSource
Questions about Dailis Pty Ltd T/a Natural Pet Treats Australia
- Is Dailis Pty Ltd T/a Natural Pet Treats Australia on an FDA import alert?
- Yes. As of October 27, 2026, Dailis Pty Ltd T/a Natural Pet Treats Australia is on the red list of FDA Import Alert 71-04, “Animal food: Salmonella”, for roo bites; green lip mussel; lamb puff ovine lung; FDA published the listing on April 1, 2025.
- Has FDA refused shipments from Dailis Pty Ltd T/a Natural Pet Treats Australia?
- No FDA import refusals for Dailis Pty Ltd T/a Natural Pet Treats Australia appear in FDA's refusal data since October 2016, as of October 27, 2026.
- What is Dailis Pty Ltd T/a Natural Pet Treats Australia's FEI number?
- Dailis Pty Ltd T/a Natural Pet Treats Australia's FDA Establishment Identifier (FEI) is 3010154895.
- Can shipments from Dailis Pty Ltd T/a Natural Pet Treats Australia still enter the U.S.?
- Shipments of roo bites; green lip mussel; lamb puff ovine lung from Dailis Pty Ltd T/a Natural Pet Treats Australia 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.