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 |
|---|---|---|---|
| Extra Large Coated Jo-Jo Wedges / 00048 (5 lb bags) | Not published in this source record | 1875 cases | Lot Codes: 170123202000048 170123203000048 170123204000048 170123205000048 170123206000048 170123207000048 170123208000048 170123211000048 170123212000048 170123214000048 170123216000048 170123217000048 170123218000048 170309201000048 170309202000048 170309203000048 170309204000048 170309205000048 170309206000048 170309207000048 170309208000048 170309209000048 170309210000048 170309211000048 170309212000048 170413205000048 170413206000048 170413208000048 170413209000048 170413210000048 170413211000048 170413212000048 170413213000048 170413214000048 170413218000048 |
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.
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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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