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Continental Canners (Pvt) Ltd.

FDA import alert and refusal historyKarachi, PakistanFEI 1000366491

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Example subjectContinental Canners (Pvt) Ltd added to Import Alert 16-129 (red list)

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As of October 26, 2026, Continental Canners (Pvt) Ltd. (Karachi, Pakistan) is on the red list of FDA Import Alert 16-81 (Seafood products: Salmonella) for shrimp, published by FDA on September 18, 2009, and has no FDA import refusals recorded since October 2016.

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

Current status

Import alerts
IA 16-81 · red list
Last import refusal
None since October 2016
Last warning letter
None found
Last inspection
None on record

Every FDA record for Continental Canners (Pvt) Ltd.

1 record, newest first. Each line links to the FDA page it came from.

2009

  1. Import alert listing
    Listed on Import Alert 16-81red listShrimp
    Source

Questions about Continental Canners (Pvt) Ltd.

Is Continental Canners (Pvt) Ltd. on an FDA import alert?
Yes. As of October 26, 2026, Continental Canners (Pvt) Ltd. is on the red list of FDA Import Alert 16-81, “Seafood products: Salmonella”, for shrimp; FDA published the listing on September 18, 2009.
Has FDA refused shipments from Continental Canners (Pvt) Ltd.?
No FDA import refusals for Continental Canners (Pvt) Ltd. appear in FDA's refusal data since October 2016, as of October 26, 2026.
What is Continental Canners (Pvt) Ltd.'s FEI number?
Continental Canners (Pvt) Ltd.'s FDA Establishment Identifier (FEI) is 1000366491.
Can shipments from Continental Canners (Pvt) Ltd. still enter the U.S.?
Shipments of shrimp from Continental Canners (Pvt) Ltd. can be detained without physical examination under Import Alert 16-81; 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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Example subjectContinental Canners (Pvt) Ltd added to Import Alert 16-129 (red list)

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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.