← FDA ENFORCEMENT
F-0405-2024Class III
The Sausage Maker, Inc.
What this record is not
A recall record is reproduced as FDA published it, and the classification is FDA’s. SPEQ adds no interpretation, and a recall concerns the products and dates in the record — it is not a statement about a company’s other products or its current status.
Recalling firm
The Sausage Maker, Inc.
Product type
Food / supplement / cosmetic
Status
Terminated
Report date
2023-11-15
Distribution
online orders nationwide
Firm state
NY
Product quantity
995 lbs.
Initiated by
Voluntary: Firm initiated
SPEQ quality domain
Environmental MonitoringReason for recall
Contains Sodium Nitrite recalled for potential metal contamination
Product description
The Sausage Maker Instacure #1
Code / lot info
Lot 30508DA010 Manf. 5/8/23 Cat No. 11-1013
Data: U.S. FDA. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification. Open the enforcement explorer →