FDA Recall United States Terminated Historical recordClass II
Penobscot McCrum LLC
- Product
- Medium Battered Jo-Jo Wedges / 00126 (5 lb bags)
- Published
- August 30, 2017
- Distribution
- Multiple states
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Policy version 2026-07-21, effective July 21, 2026.
United States
TerminatedClass II
Product may contain undeclared milk.
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Medium Coated Jo-Jo Wedges / 00040 (5lb bags) | Not published in this source record | 951 cases | Lot Codes: 170117102000040 170117103000040 170117106000040 170117109000040 170117110000040 170117111000040 170117201000040 170228101000040 170228105000040 170228106000040 170228107000040 170228108000040 170228110000040 170412206000040 170412207000040 170412208000040 170412210000040 170412213000040 170412214000040 170412216000040 |
This recall shares FDA event ID 77477 with 9 other product entries in Public Health Trace.
FDA Recall United States Terminated Historical recordClass II
FDA Recall United States Terminated Historical recordClass II
FDA Recall United States Terminated Historical recordClass II
FDA Recall United States Terminated Historical recordClass II
FDA Recall United States Terminated Historical recordClass II
FDA Recall United States Terminated Historical recordClass II
FDA Recall United States Terminated Historical recordClass II
FDA Recall United States Terminated Historical recordClass II
FDA Recall United States Terminated Historical recordClass II
Responsible company: Penobscot McCrum LLC
FDA Recall United States Terminated Historical recordClass II
FDA Recall United States Terminated Historical recordClass II
FDA Recall United States Terminated Historical 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 |
|---|---|
| Louisiana | 1 |
| Pennsylvania | 1 |
| Ohio | 1 |
| Illinois | 1 |
| Kentucky | 1 |
| Indiana | 1 |
| Tennessee | 1 |
| Texas | 1 |
| Florida | 1 |
| South Carolina | 1 |
| Colorado | 1 |
| California | 1 |
| Arkansas | 1 |
| North Carolina | 1 |
| Minnesota | 1 |
| Maine | 1 |
| Alabama | 1 |
| Michigan | 1 |
| Virginia | 1 |
| New York | 1 |
| Iowa | 1 |
| New Jersey | 1 |
| Massachusetts | 1 |
| Mississippi | 1 |
| Georgia | 1 |
| Wisconsin | 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.
No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
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.
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