RecallHawk
Class I Recall

Dried Herring Fish 7 oz.

Prime Food Processing LLC.

Summary

The FDA issued a Class I for Dried Herring Fish 7 oz. by Prime Food Processing LLC.. Reason: Improperly eviscerated which may result in Clostridium botulinum contamination.

Details

Source

Food Recall

External ID

H-1080-2026

Action Date

2026-07-01

Status

Ongoing

Category

food

Product Description

Dried Herring Fish 7 oz.

Lot/Code Info: Lot Code: 26020. Expiration: 06.12.28 UPC Codes: 6946976817911

Quantity Affected: 69 cases

Reason for Recall

Improperly eviscerated which may result in Clostridium botulinum contamination

Distribution

AZ, CA, FL, HI, IL, KS, LA, MD, MO, NC, NH, NV, NY, OK, OR, PA, TX, UT, WA

Type: Voluntary: Firm initiated

Recall Initiated: 2026-06-02

Company

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 58 food recalls issued in the same week, part of 101 food-related FDA actions this month.

Prime Food Processing LLC. has 4 FDA actions in our database, including 4 recalls.

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 (Prime Food Processing LLC.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Prime Food Processing LLC. have FDA actions?

Prime Food Processing LLC. has 4 FDA actions in our database, including 4 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "H-1080-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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