Unilever Manufacturera S. de R.L. de C.V.
FDA import alert and refusal historyLerma, MexicoFEI 3011613596
As of October 26, 2026, Unilever Manufacturera S. de R.L. de C.V. (Lerma, Mexico) is on the red list of FDA Import Alert 99-39 (Imported foods that appear to be misbranded) for flex margarine red; flex margarine blue, published by FDA on October 2, 2015, is also listed on Import Alert 45-02 (red list), 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 99-39 · red listIA 45-02 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Unilever Manufacturera S. de R.L. de C.V.
2 records, newest first. Each line links to the FDA page it came from.
2015
- Import alert listingListed on Import Alert 99-39red listFlex Margarine Red; Flex Margarine BlueSource
2009
- Import alert listingListed on Import Alert 45-02red listGelatin, FlavoredSource
Questions about Unilever Manufacturera S. de R.L. de C.V.
- Is Unilever Manufacturera S. de R.L. de C.V. on an FDA import alert?
- Yes. As of October 26, 2026, Unilever Manufacturera S. de R.L. de C.V. is on the red list of FDA Import Alert 99-39, “Imported foods that appear to be misbranded”, for flex margarine red; flex margarine blue; FDA published the listing on October 2, 2015.
- Has FDA refused shipments from Unilever Manufacturera S. de R.L. de C.V.?
- No FDA import refusals for Unilever Manufacturera S. de R.L. de C.V. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Unilever Manufacturera S. de R.L. de C.V.'s FEI number?
- Unilever Manufacturera S. de R.L. de C.V.'s FDA Establishment Identifier (FEI) is 3011613596.
- Can shipments from Unilever Manufacturera S. de R.L. de C.V. still enter the U.S.?
- Shipments of flex margarine red; flex margarine blue from Unilever Manufacturera S. de R.L. de C.V. 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.