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Caesar Lorentz

FDA import alert and refusal historyHilden, GermanyFEI 1000187439

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Example subjectCaesar Lorent added to Import Alert 16-129 (red list)

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As of October 26, 2026, Caesar Lorentz (Hilden, Germany) is on the red list of FDA Import Alert 99-19 (Food products: Salmonella) for sage, whole (spice); vitamin, n.e.c., prompt release tablets; senna leaf whole, published by FDA on September 16, 2009, and has no FDA import refusals recorded since October 2016.

Data from FDA public records, last checked . Request a correction

Current status

Last import refusal
None since October 2016
Last warning letter
None found
Last inspection
None on record

Every FDA record for Caesar Lorentz

1 record, newest first. Each line links to the FDA page it came from.

2009

  1. Import alert listing
    Listed on Import Alert 99-19red listSage, Whole (Spice); Vitamin, N.E.C., Prompt Release Tablets; senna leaf whole
    Source

Questions about Caesar Lorentz

Is Caesar Lorentz on an FDA import alert?
Yes. As of October 26, 2026, Caesar Lorentz is on the red list of FDA Import Alert 99-19, “Food products: Salmonella”, for sage, whole (spice); vitamin, n.e.c., prompt release tablets; senna leaf whole; FDA published the listing on September 16, 2009.
Has FDA refused shipments from Caesar Lorentz?
No FDA import refusals for Caesar Lorentz appear in FDA's refusal data since October 2016, as of October 26, 2026.
What is Caesar Lorentz's FEI number?
Caesar Lorentz's FDA Establishment Identifier (FEI) is 1000187439.
Can shipments from Caesar Lorentz still enter the U.S.?
Shipments of sage, whole (spice); vitamin, n.e.c., prompt release tablets; senna leaf whole from Caesar Lorentz can be detained without physical examination under Import Alert 99-19; 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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Example subjectCaesar Lorent added to Import Alert 16-129 (red list)

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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.