Agropalm Pack Sc de RL de CV

3 records, newest first. Each line links to the FDA page it came from.

Refusal charges, in plain English

• INSANITARY1 refused line

  Prepared, packed or held under insanitary conditions

  The product appeared to have been prepared, packed, or held under insanitary conditions whereby it may have been contaminated with filth or rendered injurious to health.

• MFR INSAN1 refused line

  Insanitary manufacturing, processing or packing

  The product appeared to have been manufactured, processed, or packed under insanitary conditions, which is a ground for refusal under section 801(a)(1) of the FD&C Act.

• PESTICIDE1 refused line

  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.

Questions about Agropalm Pack Sc de RL de CV

Is Agropalm Pack Sc de RL de CV on an FDA import alert?

Yes. As of October 26, 2026, Agropalm Pack Sc de RL de CV is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for green beans; FDA published the listing on September 1, 2010.

Has FDA refused shipments from Agropalm Pack Sc de RL de CV?

Yes. FDA refused 2 shipment lines from Agropalm Pack Sc de RL de CV between April 7, 2017 and December 1, 2021. The most recent, on December 1, 2021, was stringbeans, charged as PESTICIDE (pesticide chemical residue).

Why did FDA refuse Agropalm Pack Sc de RL de CV's shipments?

The most frequent charges are INSANITARY (prepared, packed or held under insanitary conditions, 1 line) and MFR INSAN (insanitary manufacturing, processing or packing, 1 line).

What is Agropalm Pack Sc de RL de CV's FEI number?

Agropalm Pack Sc de RL de CV's FDA Establishment Identifier (FEI) is 3013673574.

Can shipments from Agropalm Pack Sc de RL de CV still enter the U.S.?

Shipments of green beans from Agropalm Pack Sc de RL de CV can be detained without physical examination under Import Alert 99-05; 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).