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
Buffalo, NY
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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