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PLG EXPORT IMPORT

⚠️ Moderate Risk

FEI: 3012753870 • Hagley Park, Saint Andrew • JAMAICA

FEI

FEI Number

3012753870

📍

Location

Hagley Park, Saint Andrew

🇯🇲

Country

JAMAICA
🏢

Address

188 Spanish Town Road, , Hagley Park, Saint Andrew, Jamaica

Moderate Risk

FDA Import Risk Assessment

37.7
LowModerateHighCritical

This firm has a moderate history of FDA import refusals. Some attention may be warranted.

Statistics

9
Total Refusals
13
Unique Violations
10/7/2016
Latest Refusal
4/30/2007
Earliest Refusal

Score Breakdown

Violation Severity
64.1×40%
Refusal Volume
37.0×30%
Recency
0.0×20%
Frequency
9.5×10%
How is this score calculated?

Proprietary Algorithm

  • 40% Violation Severity — AI-assessed (1-10)
  • 30% Refusal Volume — Logarithmic scale
  • 20% Recency — Decays over 5 years
  • 10% Frequency — Refusals per year

© ImportRefusal.com Original Analysis

Violation Summary

4823×

NUTRIT LBL

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be misbranded in that the label or labeling fails to bear the required nutrition information.

2412×

PESTICIDE

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain a pesticide chemical residue, which causes the article to be adulterated within the meaning of section 402(a)(2)(B) of the FD&C Act. Bears or contains:

3212×

LACKS N/C

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(e)(2) of the FD&C Act in that the food is in package form and the label fails to bear an accurate statement of the quantity of the contents in terms of weight, measure, or numerical count in accordance with Section 403(e)(2) of the FD&C Act.

3061×

INSANITARY

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to have been prepared, packed, or held under insanitary conditions whereby it may have become contaminated with filth, or whereby it may have been rendered injurious to health.

3201×

LACKS FIRM

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(e)(1) of the FD&C Act in that the food is in package form and the label fails to bear the name and place of business of the manufacturer, packer, or distributor.

37411×

FRNMFGREG

The article is subject to refusal of admission pursuant to section 801(o) in that it is being imported or offered for import into the United States, and the importer, owner, or consignee of such article did not, at the time of offering the article for import, submit to the Secretary a statement that identifies the registration under section 510(i) of the Act of each establishment that with respect to such article is required under such section to register with the Secretary.

621×

NEEDS FCE

It appears the manufacturer is not registered as a low acid canned food or acidified food manufacturer pursuant to 21 CFR 108.25(c)(1) or 108.35(c)(1).

751×

UNAPPROVED

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a new drug within the meaning of Section 201(p) without an approved New Drug Application (NDA).

831×

NO PROCESS

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the manufacturer's failure to file a scheduled process demonstrates that the product is not being manufactured under the mandatory provisions of 21 CFR Part 108 and therefore appears to have been manufactured, processed, or packed, under insanitary conditions whereby it may have been rendered injurious to health.

111×

UNSAFE COL

The article appears to be, or to bear or contain a color additive which is unsafe within the meaning of Section 721(a).

91×

SALMONELLA

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain Salmonella, a poisonous and deleterious substance which may render it injurious to health.

1181×

NOT LISTED

It appears the drug or device is not included in a list required by Section 510(j), or a notice or other information respecting it was not provided as required by section 510(j) or 510(k).

161×

DIRECTIONS

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it is a device whose label appears to not bear adequate directions for use.

Refusal History

DateProductViolationsDivision
10/7/2016
21XET13ACKEES (SUBTROPICAL/TROPICAL FRUIT PULP)
306INSANITARY
Division of Northeast Imports (DNEI)
4/26/2013
66YCY99EXHIBITS - OTHER DRUG RELATED ITEMS N.E.C.
118NOT LISTED
16DIRECTIONS
3741FRNMFGREG
75UNAPPROVED
Division of Northeast Imports (DNEI)
3/29/2012
25JFC12SWEET POTATO (ROOT & TUBER VEGETABLE)
241PESTICIDE
Florida District Office (FLA-DO)
2/27/2012
25JFC12SWEET POTATO (ROOT & TUBER VEGETABLE)
241PESTICIDE
Florida District Office (FLA-DO)
7/7/2011
38CFT99DRIED SOUP, N.E.C.
482NUTRIT LBL
Florida District Office (FLA-DO)
7/7/2011
38CFT99DRIED SOUP, N.E.C.
321LACKS N/C
482NUTRIT LBL
Florida District Office (FLA-DO)
7/7/2011
38CFT99DRIED SOUP, N.E.C.
11UNSAFE COL
321LACKS N/C
482NUTRIT LBL
Florida District Office (FLA-DO)
9/3/2009
24FFB08PEPPER, HOT, N.E.C. (FRUIT USED AS VEGETABLE)
320LACKS FIRM
9SALMONELLA
Florida District Office (FLA-DO)
4/30/2007
37JCE02BARBECUE SAUCE
62NEEDS FCE
83NO PROCESS
Florida District Office (FLA-DO)

Frequently Asked Questions

What is PLG EXPORT IMPORT's FDA import refusal history?

PLG EXPORT IMPORT (FEI: 3012753870) has 9 FDA import refusal record(s) in our database, spanning from 4/30/2007 to 10/7/2016.

What is an FEI number?

FEI stands for Firm Establishment Identifier. It's a unique number assigned by the FDA to identify establishments that manufacture, process, pack, or hold food, drugs, medical devices, or other FDA-regulated products. PLG EXPORT IMPORT's FEI number is 3012753870.

What types of violations has PLG EXPORT IMPORT received?

PLG EXPORT IMPORT has been cited for 13 different violation type(s). Common FDA violations include adulteration (unsafe or unsanitary products), misbranding (incorrect or misleading labels), and regulatory non-compliance.

Where does this information about PLG EXPORT IMPORT come from?

All FDA import refusal data for PLG EXPORT IMPORT is sourced from the official FDA Data Dashboard (datadashboard.fda.gov), a public government database maintained by the U.S. Food and Drug Administration.

Data sourced from the FDA Data Dashboard, a public database maintained by the U.S. Food and Drug Administration.