Salted Smoked Split Herring, approximately 12 inches in length; packaged in 18 lb wooden box and repacked at retail in d
Summary
The FDA issued a Class I for Salted Smoked Split Herring, approximately 12 inches in length; packaged in 18 l by P East Trading Corp. Reason: Clostridium botulinum (uneviscerated fish).
Details
Source
Food Recall
External ID
H-0067-2025
Action Date
2025-07-02
Status
Terminated
Category
food
Product Description
Salted Smoked Split Herring, approximately 12 inches in length; packaged in 18 lb wooden box and repacked at retail in deli-style or other retail packaging (for a list of retail locations see associated press release)
Lot/Code Info: Lot: 1PRC5073
Quantity Affected: 81 cases
Reason for Recall
Clostridium botulinum (uneviscerated fish)
Distribution
NY, NJ, CT
Type: Voluntary: Firm initiated
Recall Initiated: 2025-06-06
Company
Bronx, NY
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 69 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
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 (P East Trading Corp) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does P East Trading Corp have FDA actions?
This is the only FDA action we have on record for P East Trading Corp in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0067-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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