Kawasho Foods USA, Inc Recall: Canned shrimp may be under-processed

🇺🇸 United States

1. April 22, 2023 - Recall initiated
2. May 31, 2023 - Reported by source
3. March 22, 2024 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-0930-2023

Event ID

92176

Status

Terminated

Classification

Class II

Company

Kawasho Foods USA, Inc

Product description

Geisha Medium Shrimp; WT 4OZ(113g)

Quantity

14,414 cases (172,968cans)

Reason

Canned shrimp may be under-processed

Recall initiation date

April 22, 2023

Report date

May 31, 2023

Classification date

Not published in this source record

Termination date

March 22, 2024

Distribution pattern

nationwide

UPC, lot, and code information

all codes and lots Best by: May 4th 2026, May 12th 2026, May16th 2026, July 13th 2026, May 16th 2026, May 20th 2026, July 15th 2026, July 20th 2026, July 28th 2026, Oct 19th 2026, Oct 21st 2026, Oct 26th 2026, Oct 27th 2026, Oct 28th 2026, Oct 31st 2026, Nov 1st 2026

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

Press Release

Source last updated

Not tracked separately from the Public Health Trace retrieval date below

Public Health Trace retrieval date

July 18, 2026 ET

Responsible company: Kawasho Foods USA, Inc

Other recalls from Kawasho Foods USA, Inc

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information. See FDA Enforcement Reports versus recall announcements for how that database differs from a press-release-style announcement.

New to reading a recall record? See how to read an FDA recall record and what recall statuses mean.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace: July 18, 2026 ET

Frequently asked questions

What does a Class II mean?

A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

Official guidance and record verification

Public Health Trace does not provide medical advice. The information below explains how to interpret this record and links to relevant official government sources. Review the linked official source for the current, authoritative information.

How to interpret this historical record

This record is preserved as published by FDA, as of March 22, 2024.

Status as reported: Terminated.

This page does not imply a current danger or a current consumer instruction -- review the official source for the most current information.

View the official FDA source

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.

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