Plantin SAS
FDA import alert and refusal historyPuymeras, FranceFEI 3002809058
As of October 25, 2026, Plantin SAS (Puymeras, France) is on the red list of FDA Import Alert 99-53 (Foods: naturally occurring toxins) for mushroom; morel; whole (button) (fungi), published by FDA on September 28, 2026, is also listed on Import Alert 25-02 (red list) and Import Alert 99-08 (red list), and has 21 FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Last import refusal
- Truffle, pieces and stems, sliced · NO PROCESS
- Last warning letter
- None found
- Last inspection
- Classified VAI (Voluntary Action Indicated)
Every FDA record for Plantin SAS
25 records, newest first. Each line links to the FDA page it came from.
2026
- Import alert listingListed on Import Alert 99-53red listMushroom; Morel; Whole (Button) (Fungi)Source
- Import refusalRefused, Truffle, pieces and stems, slicedNO PROCESSEntry AQZ-0649565-2Source
- Import refusalRefused, Mushroom, morel, fungi products, n.e.c.POISONOUSEntry 231-6279595-6Source
2022
- Import refusalSource
- Import refusalRefused, Truffle, pieces and stems, slicedNUTRIT LBLNEEDS FCENO PROCESSEntry MH9-2119712-4Source
- Import refusalRefused, Mushrooms and other fungi products, whole (button), n.e.c.PESTICIDEPOISONOUSFALSEEntry F23-9274144-3Source
- Import refusalSource
Refused, 4 lines in one entry: Mushrooms and other fungi products, whole (button), n.e.c.PESTICIDEEntry F23-9271032-3Show 4 linesHide lines
- Refused, Mushrooms and other fungi products, whole (button), n.e.c.PESTICIDEEntry F23-9271032-3Source
- Refused, Mushrooms and other fungi products, whole (button), n.e.c.PESTICIDEEntry F23-9271032-3Source
- Refused, Mushrooms and other fungi products, whole (button), n.e.c.PESTICIDEEntry F23-9271032-3Source
- Refused, Mushrooms and other fungi products, whole (button), n.e.c.PESTICIDEEntry F23-9271032-3Source
2019
2018
- Import refusalSource
Refused, 5 lines in one entry: Mushrooms and other fungi products, whole (button), n.e.c.; Mushroom, morel, whole (button) (fungi)PESTICIDEPOISONOUSFALSEEntry F23-9212638-9Show 5 linesHide lines
- Refused, Mushrooms and other fungi products, whole (button), n.e.c.PESTICIDEEntry F23-9212638-9Source
- Refused, Mushrooms and other fungi products, whole (button), n.e.c.PESTICIDEEntry F23-9212638-9Source
- Refused, Mushrooms and other fungi products, whole (button), n.e.c.PESTICIDEEntry F23-9212638-9Source
- Refused, Mushroom, morel, whole (button) (fungi)PESTICIDEPOISONOUSFALSEEntry F23-9212638-9Source
- Refused, Mushrooms and other fungi products, whole (button), n.e.c.PESTICIDEEntry F23-9212638-9Source
- Import refusalRefused, Mushrooms and other fungi products, whole (button), n.e.c.PESTICIDEEntry F23-9198859-9Source
- Import refusalSource
2017
- Import refusalSource
Refused, 2 lines in one entry: Truffle, fungi products, n.e.c.NUTRIT LBLNO PROCESSEntry F23-9169629-1Show 2 linesHide lines
- Refused, Truffle, fungi products, n.e.c.NUTRIT LBLNO PROCESSEntry F23-9169629-1Source
- Refused, Truffle, fungi products, n.e.c.NUTRIT LBLNO PROCESSEntry F23-9169629-1Source
2011
- InspectionInspection classified VAI (Voluntary Action Indicated)Foodborne Biological HazardsSource
2009
- Import alert listingListed on Import Alert 25-02red listMushroom, Morel, Whole (Button) (Fungi), Raw, Fresh, Refrigerated; Mushroom, Morel, Whole (Button) (Fungi), Commercially Sterile; Mushroom, Morel, Whole (Button) (Fungi), Ntrl/Artfcl DriedSource
Show 1 earlier record (2009)Hide earlier records
2009
- Import alert listingListed on Import Alert 99-08red listdried mushroomsSource
Refusal charges, in plain English
- PESTICIDE16 refused lines
Pesticide chemical residue
The product appeared to contain a pesticide chemical residue that makes it adulterated under section 402(a)(2)(B) of the FD&C Act, for example a residue above the U.S. tolerance or one with no U.S. tolerance for that food.
- POISONOUS5 refused lines
Poisonous or deleterious substance
The product appeared to bear or contain a poisonous or deleterious substance which may render it injurious to health.
- NO PROCESS4 refused lines
No scheduled process filed
The manufacturer appeared not to have filed a scheduled process with FDA, which 21 CFR Part 108 requires for low-acid canned and acidified foods, so the product is treated as made under insanitary conditions.
- FALSE3 refused lines
False or misleading labeling
The labeling appeared to be false or misleading in some particular.
- NUTRIT LBL3 refused lines
Nutrition information missing from label
The label or labeling appeared not to carry the nutrition information that U.S. law requires for the food.
- NEEDS FCE1 refused line
Processor not registered for canned or acidified foods
The manufacturer appeared not to be registered with FDA as a low-acid canned food or acidified food processor, as 21 CFR 108.25 and 108.35 require.
Questions about Plantin SAS
- Is Plantin SAS on an FDA import alert?
- Yes. As of October 25, 2026, Plantin SAS is on the red list of FDA Import Alert 99-53, “Foods: naturally occurring toxins”, for mushroom; morel; whole (button) (fungi); FDA published the listing on September 28, 2026.
- Has FDA refused shipments from Plantin SAS?
- Yes. FDA refused 21 shipment lines from Plantin SAS between June 8, 2017 and June 15, 2026. The most recent, on June 15, 2026, was truffle, pieces and stems, sliced, charged as NO PROCESS (no scheduled process filed).
- Why did FDA refuse Plantin SAS's shipments?
- The most frequent charges are PESTICIDE (pesticide chemical residue, 16 lines) and POISONOUS (poisonous or deleterious substance, 5 lines).
- When was Plantin SAS last inspected by FDA?
- FDA's most recent inspection of Plantin SAS with a final classification is dated May 13, 2011 and was classified VAI (Voluntary Action Indicated).
- What is Plantin SAS's FEI number?
- Plantin SAS's FDA Establishment Identifier (FEI) is 3002809058.
- Can shipments from Plantin SAS still enter the U.S.?
- Shipments of mushroom; morel; whole (button) (fungi) from Plantin SAS can be detained without physical examination under Import Alert 99-53; 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.