Label reads in part: TWIN FIN DELI; Salami; Net WT. 1lb (453g); P.O. Box 399 Thomson IL, FDA#…
Recalling firm: Schafer Fisheries
Lack of adequate HACCP records.
Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: May 30, 2018.
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FDA code information
Bar Code Number: 4278600054; Lot Number: 14278, 11945, 12562, 12509, 12304, 12429, 12395r, 12489, 12750, 12773, 12394, 12380, 11944, 12312, 12002, 12172, 12763.; Manufacture date: 7/2/2013, 7/23/2013.
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Full FDA record and distribution details
Original product description
Label reads in part: TWIN FIN DELI; Salami; Net WT. 1lb (453g); P.O. Box 399 Thomson IL, FDA# 1481764 Thomason
Extracted codes and context
| Type | Code / value | Context |
|---|---|---|
| lot | 11944 | , 11945, 12562, 12509, 12304, 12429, 12395r, 12489, 12750, 12773, 12394, 12380, 11944, 12312, 12002, 12172, 12763.; Manufacture date: 7/2/2013, 7/23/2013. |
| lot | 11945 | Bar Code Number: 4278600054; Lot Number: 14278, 11945, 12562, 12509, 12304, 12429, 12395r, 12489, 12750, 12773, 12394, 12380, 11944, 12312, 12002, 12172, 12763.; Manufacture |
| lot | 12002 | , 12509, 12304, 12429, 12395r, 12489, 12750, 12773, 12394, 12380, 11944, 12312, 12002, 12172, 12763.; Manufacture date: 7/2/2013, 7/23/2013. |
| lot | 12172 | , 12304, 12429, 12395r, 12489, 12750, 12773, 12394, 12380, 11944, 12312, 12002, 12172, 12763.; Manufacture date: 7/2/2013, 7/23/2013. |
| lot | 12304 | Bar Code Number: 4278600054; Lot Number: 14278, 11945, 12562, 12509, 12304, 12429, 12395r, 12489, 12750, 12773, 12394, 12380, 11944, 12312, 12002, 12172, 12763.; Manufacture date: 7/2/2013, 7/23 |
| lot | 12312 | , 12562, 12509, 12304, 12429, 12395r, 12489, 12750, 12773, 12394, 12380, 11944, 12312, 12002, 12172, 12763.; Manufacture date: 7/2/2013, 7/23/2013. |
| lot | 12380 | : 14278, 11945, 12562, 12509, 12304, 12429, 12395r, 12489, 12750, 12773, 12394, 12380, 11944, 12312, 12002, 12172, 12763.; Manufacture date: 7/2/2013, 7/23/2013. |
| lot | 12394 | Number: 14278, 11945, 12562, 12509, 12304, 12429, 12395r, 12489, 12750, 12773, 12394, 12380, 11944, 12312, 12002, 12172, 12763.; Manufacture date: 7/2/2013, 7/23/2013. |
| lot | 12395r | de Number: 4278600054; Lot Number: 14278, 11945, 12562, 12509, 12304, 12429, 12395r, 12489, 12750, 12773, 12394, 12380, 11944, 12312, 12002, 12172, 12763.; Manufacture date: 7/2/2013, 7/23/2013. |
| lot | 12429 | Bar Code Number: 4278600054; Lot Number: 14278, 11945, 12562, 12509, 12304, 12429, 12395r, 12489, 12750, 12773, 12394, 12380, 11944, 12312, 12002, 12172, 12763.; Manufacture date: 7/2/2013, 7/23/2013. |
| lot | 12489 | r: 4278600054; Lot Number: 14278, 11945, 12562, 12509, 12304, 12429, 12395r, 12489, 12750, 12773, 12394, 12380, 11944, 12312, 12002, 12172, 12763.; Manufacture date: 7/2/2013, 7/23/2013. |
| lot | 12509 | Bar Code Number: 4278600054; Lot Number: 14278, 11945, 12562, 12509, 12304, 12429, 12395r, 12489, 12750, 12773, 12394, 12380, 11944, 12312, 12002, 12172, 12763.; Manufacture date: 7/2/201 |
| lot | 12562 | Bar Code Number: 4278600054; Lot Number: 14278, 11945, 12562, 12509, 12304, 12429, 12395r, 12489, 12750, 12773, 12394, 12380, 11944, 12312, 12002, 12172, 12763.; Manufacture date: |
| lot | 12750 | 8600054; Lot Number: 14278, 11945, 12562, 12509, 12304, 12429, 12395r, 12489, 12750, 12773, 12394, 12380, 11944, 12312, 12002, 12172, 12763.; Manufacture date: 7/2/2013, 7/23/2013. |
| lot | 12773 | ; Lot Number: 14278, 11945, 12562, 12509, 12304, 12429, 12395r, 12489, 12750, 12773, 12394, 12380, 11944, 12312, 12002, 12172, 12763.; Manufacture date: 7/2/2013, 7/23/2013. |
| lot | 14278 | Bar Code Number: 4278600054; Lot Number: 14278, 11945, 12562, 12509, 12304, 12429, 12395r, 12489, 12750, 12773, 12394, 12380, 11944, 12312, 12002, 12172, 12763.; Manu |
Original FDA recall reason
Lack of adequate HACCP records.
Recall details
- Recall number
- F-0040-2017
- Event ID
- 66278
- FDA status
- Terminated
- Initiated
- Aug 22, 2013
- Reported
- Oct 19, 2016
- Classified
- Oct 7, 2016
- Terminated
- May 30, 2018
- Quantity
- 398 cases (12 units per case)
- Location
- FULTON, IL, United States
- Initiation type
- Voluntary: Firm initiated
- Notification
- Telephone
Where it was distributed
US: IL, NY, CA
Data updated September 16, 2026. View official FDA data ↗
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