RecallHawk
Class I Recall

Lemon Dill Butter Pucks

Raw Seafoods Inc.

Summary

The FDA issued a Class I for Lemon Dill Butter Pucks by Raw Seafoods Inc.. Reason: Firm used dill recalled for Listeria monocytogenes to product butter pucks.

Details

Source

Food Recall

External ID

F-1583-2022

Action Date

2022-09-07

Status

Terminated

Category

food

Product Description

Lemon Dill Butter Pucks

Lot/Code Info: Lot/Unit Numbers: B5123 Expiration date(s) or Use by Date(s) or expected shelf life of product: 07/19/2023 UPC Codes: 10889396002907

Quantity Affected: 2 cases

Reason for Recall

Firm used dill recalled for Listeria monocytogenes to product butter pucks

Distribution

OH, MA

Type: Voluntary: Firm initiated

Recall Initiated: 2022-08-11

Company

Raw Seafoods Inc.

Fall River, MA

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 111 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Raw Seafoods Inc. has 3 FDA actions in our database, including 3 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 (Raw Seafoods Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Raw Seafoods Inc. have FDA actions?

Raw Seafoods Inc. has 3 FDA actions in our database, including 3 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-1583-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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