Is Vicente Acosta Cid on an FDA import alert?

No listing for Vicente Acosta Cid appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Mexico page.

Has FDA refused shipments from Vicente Acosta Cid?

Yes. FDA refused 6 shipment lines from Vicente Acosta Cid between July 28, 2023 and August 9, 2023. The most recent, on August 9, 2023, was hami melon, charged as INSANITARY (prepared, packed or held under insanitary conditions).

Why did FDA refuse Vicente Acosta Cid's shipments?

The most frequent charges are INSANITARY (prepared, packed or held under insanitary conditions, 6 lines) and MFR INSAN (insanitary manufacturing, processing or packing, 6 lines).

What is Vicente Acosta Cid's FEI number?

Vicente Acosta Cid's FDA Establishment Identifier (FEI) is 3019789422.

Vicente Acosta Cid

FDA import alert and refusal historySan Luis Rio Colorado, MexicoFEI 3019789422

Recorded by FDA as VICENTE ACOSTA CID

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As of October 26, 2026, Vicente Acosta Cid is not on any FDA import alert in SupplierRadar's records; FDA refused 6 of its shipment lines between July 28, 2023 and August 9, 2023, most often for prepared, packed or held under insanitary conditions (INSANITARY).

Data from FDA public records, last checked October 26, 2026. Request a correction

Current status

Import alerts: Not listed
Last import refusal: Aug 9, 2023Hami melon · INSANITARY
Last warning letter: None found
Last inspection: None on record

Every FDA record for Vicente Acosta Cid

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

2023

Aug 9, 2023Import refusal
Refused, 2 lines in one entry: Hami melonINSANITARYMFR INSANSALMONELLAEntry 8E5-2314385-8Show 2 linesHide lines
- Refused, Hami melonINSANITARY MFR INSAN SALMONELLAEntry 8E5-2314385-8Source
- Refused, Hami melonINSANITARY MFR INSAN SALMONELLAEntry 8E5-2314385-8Source
Source
Jul 28, 2023Import refusal
Refused, Hami melonINSANITARY MFR INSAN SALMONELLAEntry 8E5-2314339-5
Source
Jul 28, 2023Import refusal
Refused, 2 lines in one entry: Hami melonINSANITARYMFR INSANSALMONELLAEntry 8E5-2314363-5Show 2 linesHide lines
- Refused, Hami melonINSANITARY MFR INSAN SALMONELLAEntry 8E5-2314363-5Source
- Refused, Hami melonINSANITARY MFR INSAN SALMONELLAEntry 8E5-2314363-5Source
Source
Jul 28, 2023Import refusal
Refused, Hami melonINSANITARY MFR INSAN SALMONELLAEntry 8E5-2314339-5
Source

Refusal charges, in plain English

INSANITARY6 refused lines
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 INSAN6 refused lines
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.
SALMONELLA6 refused lines
Salmonella
The product appeared to contain Salmonella, which the law treats as a poisonous and deleterious substance that may make food injurious to health.

Questions about Vicente Acosta Cid

Is Vicente Acosta Cid on an FDA import alert?: No listing for Vicente Acosta Cid appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Mexico page.
Has FDA refused shipments from Vicente Acosta Cid?: Yes. FDA refused 6 shipment lines from Vicente Acosta Cid between July 28, 2023 and August 9, 2023. The most recent, on August 9, 2023, was hami melon, charged as INSANITARY (prepared, packed or held under insanitary conditions).
Why did FDA refuse Vicente Acosta Cid's shipments?: The most frequent charges are INSANITARY (prepared, packed or held under insanitary conditions, 6 lines) and MFR INSAN (insanitary manufacturing, processing or packing, 6 lines).
What is Vicente Acosta Cid's FEI number?: Vicente Acosta Cid's FDA Establishment Identifier (FEI) is 3019789422.

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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.