Skjodt-Barrett Foods
FDA import alert and refusal historyBrampton, CanadaFEI 3010811909
As of October 26, 2026, Skjodt-Barrett Foods (Brampton, Canada) is on the red list of FDA Import Alert 99-39 (Imported foods that appear to be misbranded) for mixed fruit purees; banana pumpkin organic baby food; mixed fruit (baby), published by FDA on October 16, 2018, and has 5 FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 99-39 · red list
- Last import refusal
- Mixed fruit purees, n.e.c. · FALSE
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Skjodt-Barrett Foods
6 records, newest first. Each line links to the FDA page it came from.
2025
2019
2018
Refusal charges, in plain English
- FALSE5 refused lines
False or misleading labeling
The labeling appeared to be false or misleading in some particular.
Questions about Skjodt-Barrett Foods
- Is Skjodt-Barrett Foods on an FDA import alert?
- Yes. As of October 26, 2026, Skjodt-Barrett Foods is on the red list of FDA Import Alert 99-39, “Imported foods that appear to be misbranded”, for mixed fruit purees; banana pumpkin organic baby food; mixed fruit (baby); FDA published the listing on October 16, 2018.
- Has FDA refused shipments from Skjodt-Barrett Foods?
- Yes. FDA refused 5 shipment lines from Skjodt-Barrett Foods between November 21, 2018 and November 14, 2025. The most recent, on November 14, 2025, was mixed fruit purees, n.e.c., charged as FALSE (false or misleading labeling).
- Why did FDA refuse Skjodt-Barrett Foods's shipments?
- The most frequent charge is FALSE (false or misleading labeling, 5 lines).
- What is Skjodt-Barrett Foods's FEI number?
- Skjodt-Barrett Foods's FDA Establishment Identifier (FEI) is 3010811909.
- Can shipments from Skjodt-Barrett Foods still enter the U.S.?
- Shipments of mixed fruit purees; banana pumpkin organic baby food; mixed fruit (baby) from Skjodt-Barrett Foods can be detained without physical examination under Import Alert 99-39; 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.