FDA recall record
The Sausage Maker Instacure #1
FDA classification. FDA Class I, II, and III are not the same as USDA FSIS classifications and are not a cross-agency safety score.
FDA listed a termination date of April 10, 2025. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
The Sausage Maker Instacure #1
Reason
Contains Sodium Nitrite recalled for potential metal contamination
Products involved
Product descriptions are copied from the FDA recall record. They are not a current catalog and are not automatically matched to WhoMadeMyFood product pages.
The Sausage Maker Instacure #1
Code information listed by FDA
Lot 30508DA010 Manf. 5/8/23 Cat No. 11-1013
Distribution and firm information
Recalling firm listed by FDA: The Sausage Maker, Inc.
Firm location listed by FDA: Buffalo, NY, United States
Distribution reported by FDA: online orders nationwide
Product quantity listed by FDA: 995 lbs.
Source
Source: U.S. Food and Drug Administration (FDA), openFDA food enforcement reports.
Official FDA openFDA food enforcement record
Identifying an FDA recall record does not imply FDA endorsement of WhoMadeMyFood. Methodology.