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 |
|---|---|---|---|
| Valero Baby Wedges with Crisp Coat UC Coating / 51049 (5 lb bags) | Not published in this source record | 5924 cases | Lot Codes: 161213201051049 161213202051049 161213203051049 161213204051049 161213205051049 161213207051049 161213208051049 161213209051049 161213210051049 161213211051049 161213212051049 161213213051049 161213215051049 161213216051049 161213217051049 161213218051049 161213219051049 161213220051049 161213221051049 161213222051049 161213223051049 161213224051049 161213225051049 170130200051049 170130201051049 170130202051049 170130203051049 170130204051049 170130205051049 170130206051049 170130207051049 170130208051049 170130209051049 170130210051049 170130212051049 170130213051049 170130214051049 170130215051049 170130216051049 170130217051049 170130218051049 170130219051049 170130220051049 170130222051049 170130223051049 170130224051049 170130225051049 170130226051049 170130227051049 170130228051049 170130229051049 170221201051049 170221202051049 170221203051049 170221204051049 170221205051049 170221206051049 170221207051049 170221208051049 170221209051049 170221210051049 170221211051049 170221212051049 170221213051049 170221214051049 170221215051049 170221216051049 170221217051049 170221218051049 170221219051049 170221220051049 170221221051049 170221222051049 170221223051049 170221224051049 170221225051049 170221226051049 170418101051049 170418103051049 170418104051049 170418105051049 170418107051049 170418108051049 170418109051049 170418111051049 170418112051049 170418116051049 170418117051049 170418119051049 170418120051049 170418125051049 170418126051049 170418201051049 170418203051049 170418209051049 170418210051049 170418211051049 170418212051049 170418213051049 170418214051049 170418217051049 170418218051049 170418219051049 170418220051049 170418221051049 170418223051049 170418224051049 170418225051049 170418226051049 |
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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