Class IITerminated in FDA datasetRecall initiated Jun 9, 2017

FPI 1/10 PAN-SEAR Chili Lime Tilapia Fillets. Item Number: 1059540

Recalling firm: High Liner Foods Inc.

Why it was recalled

Product may contain undeclared milk.

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: Dec 14, 2017.

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ProductFPI 1/10 PAN-SEAR Chili Lime Tilapia Fillets. Item Number: 1059540

FDA code information

Lot Number: 0027028170; 0027081260; 0027050160; 0027111110; 0027067160; 0027028270; 0027096110; 0027067260; 0027050260

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Full FDA record and distribution details

Original product description

FPI 1/10 PAN-SEAR Chili Lime Tilapia Fillets. Item Number: 1059540

Extracted codes and context

TypeCode / valueContext
lot0027028170Lot Number: 0027028170; 0027081260; 0027050160; 0027111110; 0027067160; 0027028270; 0027096110; 0027067260; 0027050260
lot0027028270Lot Number: 0027028170; 0027081260; 0027050160; 0027111110; 0027067160; 0027028270; 0027096110; 0027067260; 0027050260
lot0027050160Lot Number: 0027028170; 0027081260; 0027050160; 0027111110; 0027067160; 0027028270; 0027096110; 0027067260; 0027050260
lot0027050260081260; 0027050160; 0027111110; 0027067160; 0027028270; 0027096110; 0027067260; 0027050260
lot0027067160Lot Number: 0027028170; 0027081260; 0027050160; 0027111110; 0027067160; 0027028270; 0027096110; 0027067260; 0027050260
lot0027067260028170; 0027081260; 0027050160; 0027111110; 0027067160; 0027028270; 0027096110; 0027067260; 0027050260
lot0027081260Lot Number: 0027028170; 0027081260; 0027050160; 0027111110; 0027067160; 0027028270; 0027096110; 0027067260; 0027050260
lot0027096110Number: 0027028170; 0027081260; 0027050160; 0027111110; 0027067160; 0027028270; 0027096110; 0027067260; 0027050260
lot0027111110Lot Number: 0027028170; 0027081260; 0027050160; 0027111110; 0027067160; 0027028270; 0027096110; 0027067260; 0027050260

Original FDA recall reason

Product may contain undeclared milk.

Recall details

Recall number
F-2752-2017
Event ID
77489
FDA status
Terminated
Initiated
Jun 9, 2017
Reported
Aug 23, 2017
Classified
Aug 15, 2017
Terminated
Dec 14, 2017
Quantity
693,408 cases (total for all products)
Location
Portsmouth, NH, United States
Initiation type
Voluntary: Firm initiated
Notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Where it was distributed

Nationwide

FDA source record · F-2752-2017

Data updated September 16, 2026. View official FDA data ↗

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