Summary
The FDA issued a Class II for Geisha Medium Shrimp; WT 4OZ(113g) by Kawasho Foods USA, Inc. Reason: Canned shrimp may be under-processed.
Details
Source
Food Recall
External ID
F-0930-2023
Action Date
2023-05-31
Status
Terminated
Category
food
Product Description
Geisha Medium Shrimp; WT 4OZ(113g)
Lot/Code Info: 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
Quantity Affected: 14,414 cases (172,968cans)
Reason for Recall
Canned shrimp may be under-processed
Distribution
nationwide
Type: Voluntary: Firm initiated
Recall Initiated: 2023-04-22
Company
New York, NY
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 71 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Kawasho Foods USA, Inc has 2 FDA actions in our database, including 2 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Kawasho Foods USA, Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Kawasho Foods USA, Inc have FDA actions?
Kawasho Foods USA, Inc has 2 FDA actions in our database, including 2 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0930-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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