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Presto

⚠️ Moderate Risk

FEI: 3003631104 • Saint-Jean-Sur-Richelieu, Quebec • CANADA

FEI

FEI Number

3003631104

📍

Location

Saint-Jean-Sur-Richelieu, Quebec

🇨🇦

Country

CANADA
🏢

Address

650 De Dijon St, , Saint-Jean-Sur-Richelieu, Quebec, Canada

Moderate Risk

FDA Import Risk Assessment

40.9
LowModerateHighCritical

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

Statistics

14
Total Refusals
7
Unique Violations
2/24/2003
Latest Refusal
2/24/2003
Earliest Refusal

Score Breakdown

Violation Severity
44.6×40%
Refusal Volume
43.6×30%
Recency
0.0×20%
Frequency
100.0×10%
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

32110×

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.

48210×

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.

2767×

PRESRV LBL

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain a chemical preservative and it fails to bear labeling stating that fact including its function.

115×

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).

2185×

LIST INGRE

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(i)(2) of the FD&C Act in that it is fabricated from two or more ingredients and the label fails to bear the common or usual name of each such ingredient and/or the article purports to be a beverage containing vegetable or fruit juice, but does not bear a statement with appropriate prominence on the information panel of the total percentage of such fruit or vegetable juice contained in the food.

3241×

NO ENGLISH

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(f) of the FD&C Act in that any word, statement, or other information required by or under the authority of the FD&C Act to appear on the label or labeling is not prominently placed thereon with such conspicuousness (as compared with other words, statements, designs, or devices, in the labeling) and in such terms as to render it likely to be read and understood by the ordinary individual under customary terms of purchase and use (for example, label contains information in two or more languages but fails to repeat all required information in both languages in accordance with 21 CFR 101.15(c)(2), or label fails to include all required information in English in accordance with 21 CFR 101.15(c)(1), except in the case of articles distributed solely in the Commonwealth of Puerto Rico or in a Territory where the predominant language is one other than English)).

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.

Refusal History

DateProductViolationsDivision
2/24/2003
37JCT99SAUCES, N.E.C.
482NUTRIT LBL
New York District Office (NYK-DO)
2/24/2003
24AGT99BEANS, CORN, AND PEA, N.E.C. (VEGETABLE)
324NO ENGLISH
New York District Office (NYK-DO)
2/24/2003
25NCE08RED BEET, WITH SAUCE
321LACKS N/C
482NUTRIT LBL
83NO PROCESS
New York District Office (NYK-DO)
2/24/2003
37JCT05SOY SAUCE
276PRESRV LBL
321LACKS N/C
482NUTRIT LBL
New York District Office (NYK-DO)
2/24/2003
27YCT01CATSUP
276PRESRV LBL
321LACKS N/C
482NUTRIT LBL
New York District Office (NYK-DO)
2/24/2003
03AGT99BREAD/ROLLS/BUNS, N.E.C.
276PRESRV LBL
321LACKS N/C
482NUTRIT LBL
New York District Office (NYK-DO)
2/24/2003
23CHT07PEANUT, BUTTER
218LIST INGRE
321LACKS N/C
482NUTRIT LBL
New York District Office (NYK-DO)
2/24/2003
21GGT05DATES (PIT FRUIT), (PIT FRUIT)
218LIST INGRE
321LACKS N/C
482NUTRIT LBL
New York District Office (NYK-DO)
2/24/2003
29BEY99CARBONATED SOFT DRINK, N.E.C.
218LIST INGRE
276PRESRV LBL
321LACKS N/C
482NUTRIT LBL
New York District Office (NYK-DO)
2/24/2003
33LGT04FONDANT CANDY PIECES, SOFT, WITHOUT NUTS AND FRUIT (WITHOUT CHOCOLATE)
11UNSAFE COL
482NUTRIT LBL
New York District Office (NYK-DO)
2/24/2003
37JCT99SAUCES, N.E.C.
11UNSAFE COL
276PRESRV LBL
482NUTRIT LBL
New York District Office (NYK-DO)
2/24/2003
33THT99TOPPINGS WITHOUT FRUIT, NUTS OR CHOCOLATE N.E.C.
11UNSAFE COL
276PRESRV LBL
321LACKS N/C
New York District Office (NYK-DO)
2/24/2003
03NGT01CAKE,CUSTARD OR CREAM FILLED
11UNSAFE COL
218LIST INGRE
321LACKS N/C
New York District Office (NYK-DO)
2/24/2003
03HFT09FRUIT/FRUIT FLAVORED PLAIN COOKIES, BISCUITS AND WAFERS
11UNSAFE COL
218LIST INGRE
276PRESRV LBL
321LACKS N/C
New York District Office (NYK-DO)

Frequently Asked Questions

What is Presto's FDA import refusal history?

Presto (FEI: 3003631104) has 14 FDA import refusal record(s) in our database, spanning from 2/24/2003 to 2/24/2003.

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. Presto's FEI number is 3003631104.

What types of violations has Presto received?

Presto has been cited for 7 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 Presto come from?

All FDA import refusal data for Presto 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.