Pollock Fillet is frozen block
Reason Frozen Pollock fillet block is recalled because one customer has found metal fragments in fillet block.
Pollock mince is frozen block recall
Recalled by GAS LLC, LLC - Golden Alaska M/V · Seattle, WA, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Frozen Pollock mince block is recalled because one customer has found metal fragments in fillet block.
Hard or sharp fragments can cut the mouth or throat, break teeth or cause choking. They usually come from equipment wear or packaging on the production line. All foreign material recalls.
What was recalled
Pollock mince is frozen block, packed in waxed coated fiber block liners. Each frozen block weighs 7.45 KG. There are 3 blocks packaged in a fiber master carton that has a poly box liner. The master case is a brown carton with blue print that has the brand "Alaska Brands" on the case and has a poly liner. This product was to be reprocessed and there are no UPC codes. Grades Mince A and MN Mince A
Quantity: 3,330 cases (22.45 kg per case)
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
Kloosterboer warehouse lot codes: D-033982 and D-033983.
Where it was sold
Massachusetts
FDA's distribution note: Distributed in MA and the following countries: Denmark, Germany, Japan, and The Netherlands.
Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- GAS LLC, LLC - Golden Alaska M/V
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Mar 30, 2017
- In FDA report of
- May 17, 2017
- Terminated
- Sep 8, 2017
- FDA recall number
- F-2188-2017 · event 76908
- Official record
- FDA enforcement report search
Also recalled with it (1 more product)
FDA files each product of one recall action separately; these share the same FDA event.