Has FDA refused shipments from Pride Pak Canada Ltd.?

Yes. FDA refused 5 shipment lines from Pride Pak Canada Ltd. between January 13, 2023 and June 25, 2024. The most recent, on June 25, 2024, was fresh shredded mixed vegetables for salads (mixed vegetables), charged as POISONOUS (poisonous or deleterious substance).

Why did FDA refuse Pride Pak Canada Ltd.'s shipments?

The most frequent charge is POISONOUS (poisonous or deleterious substance, 5 lines).

What is Pride Pak Canada Ltd.'s FEI number?

Pride Pak Canada Ltd.'s FDA Establishment Identifier (FEI) is 3003146529.

Can shipments from Pride Pak Canada Ltd. still enter the U.S.?

Shipments of french blend salad; green leaf lettuce; frisee; radicchio & shredded carrots from Pride Pak Canada Ltd. can be detained without physical examination under Import Alert 99-42; 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).

Pride Pak Canada Ltd.

FDA import alert and refusal historyMississauga, CanadaFEI 3003146529

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As of October 25, 2026, Pride Pak Canada Ltd. (Mississauga, Canada) is on the red list of FDA Import Alert 99-42 (Foods: heavy metal (toxic element) contamination) for french blend salad; green leaf lettuce; frisee; radicchio & shredded carrots, published by FDA on January 27, 2023, and has 5 FDA import refusals recorded since October 2016.

Data from FDA public records, last checked October 25, 2026. Request a correction

Current status

Import alerts: IA 99-42 · red list
Last import refusal: Jun 25, 2024Fresh shredded mixed vegetables for salads (mixed vegetables) · POISONOUS
Last warning letter: None found
Last inspection: None on record

Every FDA record for Pride Pak Canada Ltd.

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

2024

Jun 25, 2024Import refusal
Refused, Fresh shredded mixed vegetables for salads (mixed vegetables)POISONOUSEntry CDF-0490584-3
Source
Jun 24, 2024Import refusal
Refused, Fresh shredded mixed vegetables for salads (mixed vegetables)POISONOUSEntry CDF-0492873-8
Source

2023

Feb 22, 2023Import refusal
Refused, Fresh shredded mixed vegetables for salads (mixed vegetables)POISONOUSEntry CDF-0439729-8
Source
Feb 22, 2023Import refusal
Refused, Fresh shredded mixed vegetables for salads (mixed vegetables)POISONOUSEntry CDF-0439678-7
Source
Jan 27, 2023Import alert listing
Listed on Import Alert 99-42red listFrench Blend Salad; Green Leaf Lettuce; Frisee; Radicchio & Shredded Carrots
Source
Jan 13, 2023Import refusal
Refused, Fresh shredded mixed vegetables for salads (mixed vegetables)POISONOUSEntry CDF-0430598-6
Source

Refusal charges, in plain English

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.

Questions about Pride Pak Canada Ltd.

Is Pride Pak Canada Ltd. on an FDA import alert?: Yes. As of October 25, 2026, Pride Pak Canada Ltd. is on the red list of FDA Import Alert 99-42, “Foods: heavy metal (toxic element) contamination”, for french blend salad; green leaf lettuce; frisee; radicchio & shredded carrots; FDA published the listing on January 27, 2023.
Has FDA refused shipments from Pride Pak Canada Ltd.?: Yes. FDA refused 5 shipment lines from Pride Pak Canada Ltd. between January 13, 2023 and June 25, 2024. The most recent, on June 25, 2024, was fresh shredded mixed vegetables for salads (mixed vegetables), charged as POISONOUS (poisonous or deleterious substance).
Why did FDA refuse Pride Pak Canada Ltd.'s shipments?: The most frequent charge is POISONOUS (poisonous or deleterious substance, 5 lines).
What is Pride Pak Canada Ltd.'s FEI number?: Pride Pak Canada Ltd.'s FDA Establishment Identifier (FEI) is 3003146529.
Can shipments from Pride Pak Canada Ltd. still enter the U.S.?: Shipments of french blend salad; green leaf lettuce; frisee; radicchio & shredded carrots from Pride Pak Canada Ltd. can be detained without physical examination under Import Alert 99-42; 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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