RecallHawk
Class III Recall

The Sausage Maker Instacure #1

The Sausage Maker, Inc.

Summary

The FDA issued a Class III for The Sausage Maker Instacure #1 by The Sausage Maker, Inc.. Reason: Contains Sodium Nitrite recalled for potential metal contamination.

Details

Source

Food Recall

External ID

F-0405-2024

Action Date

2023-11-15

Status

Terminated

Category

food

Product Description

The Sausage Maker Instacure #1

Lot/Code Info: Lot 30508DA010 Manf. 5/8/23 Cat No. 11-1013

Quantity Affected: 995 lbs.

Reason for Recall

Contains Sodium Nitrite recalled for potential metal contamination

Distribution

online orders nationwide

Type: Voluntary: Firm initiated

Recall Initiated: 2023-07-25

Company

Context & Analysis

This is a Class III recall. Class III recalls involve products unlikely to cause adverse health consequences, but that violate FDA regulations.

This was one of 106 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Frequently Asked Questions

What is a Class III recall?

A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.

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 (The Sausage Maker, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does The Sausage Maker, Inc. have FDA actions?

This is the only FDA action we have on record for The Sausage Maker, Inc. in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0405-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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