FDA Recall United States TerminatedTerminated: March 21, 2024Historical recordClass II
Mennel Milling Company
- Product
- PIZZA 50/50 UNMALTED 904181 delivered as bulk product in app…
- Published
- February 28, 2024
- Distribution
- Multiple states
United States
TerminatedClass II
Potential Foreign Material - Metal, Wood, Gasket Material, and/or Sifter balls
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| 1002560 DONUT CAKE FLR delivered as bulk product in approximately 50,000 lbs trailers | Not published in this source record | 2633960 TOTAL lbs | Lot Codes: 24024-43; 24024-46; 24024-51; 24024-55; 24025-04; 24025-17; 24025-11; 24025-14; 24025-07; 24025-33; 24025-40; 24025-37; 24026-10; 24026-24; 24026-26; 24026-05; 24026-19; 24025-46; 24027-14; 24027-19; 24027-11; 24026-38; 24027-04; 24027-25; 24029-03; 24028-19; 24027-06; 24027-05; 24026-12; 24028-07; 24026-23; 24028-10; 24026-53; 24025-35; 24026-20; 24026-15; 24028-18 Product Code: RM48P1-00356 |
This recall shares FDA event ID 93915 with 10 other product entries in Public Health Trace.
FDA Recall United States TerminatedTerminated: March 21, 2024Historical recordClass II
FDA Recall United States TerminatedTerminated: March 21, 2024Historical recordClass II
FDA Recall United States TerminatedTerminated: March 21, 2024Historical recordClass II
FDA Recall United States TerminatedTerminated: March 21, 2024Historical recordClass II
FDA Recall United States TerminatedTerminated: March 21, 2024Historical recordClass II
FDA Recall United States TerminatedTerminated: March 21, 2024Historical recordClass II
FDA Recall United States TerminatedTerminated: March 21, 2024Historical recordClass II
FDA Recall United States TerminatedTerminated: March 21, 2024Historical recordClass II
FDA Recall United States TerminatedTerminated: March 21, 2024Historical recordClass II
FDA Recall United States TerminatedTerminated: March 21, 2024Historical recordClass II
Responsible company: Mennel Milling Company
FDA Recall United States TerminatedTerminated: March 21, 2024Historical recordClass II
FDA Recall United States TerminatedTerminated: March 21, 2024Historical recordClass II
FDA Recall United States TerminatedTerminated: March 21, 2024Historical recordClass II
A map highlighting the states named in the source's distribution description.
Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.
| State | Distributed |
|---|---|
| Kentucky | 1 |
| Michigan | 1 |
| New Jersey | 1 |
| New York | 1 |
| Ohio | 1 |
| Pennsylvania | 1 |
States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.
View FDA enforcement record -- the specific openFDA record this summary was built from.
This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.
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View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.
According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.
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This record is preserved as published by FDA, as of March 21, 2024.
Status as reported: Terminated.
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