Buckhead Tuna
Reason The Firm was notified by NJ Department of Health of two samples collected from tuna with reported high levels of scombrotoxin.
Canned Salmon in unlabeled recall
Recalled by YWAM Faith Harvest Helpers · Olympia, WA, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
All canned salmon manufactured by YWAM Faith Harvest Helpers is recalled due to the firm not having a scheduled process for manufacturing the low-acid canned food product.
These are failures of the safety steps that keep food safe - cooking, pasteurising, keeping cold, sealing - even when no contaminant has yet been found. All processing & sanitation problems recalls.
What was recalled
Canned Salmon in unlabeled 8oz metal cans. Cans are packaged into a case of 92 cans. The case label is read: "Canned Salmon***Product of U.S.A. Net. Wt. 62 lbs. Packed by: Faith Harvest Helpers 12643 Case Rd SW Olympia, WA 98512***"
Quantity: 4,818/8 oz. cans
Food: Seafood & fish
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.
The product can be traced from an unopened labeled case of canned salmon. If the case has been open, there is no way to distinguish the difference between good and bad. The can is a solid color with no labeling or coding. Exp. 1/11/21, 1/12/21, 2/7/21, 2/25/21.
Where it was sold
North Dakota Washington Wyoming
FDA's distribution note: Distributed to tribes in Washington, North Dakota, Wyoming, and in Guatemala.
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
- YWAM Faith Harvest Helpers
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Jul 5, 2018
- In FDA report of
- Aug 15, 2018
- Terminated
- Nov 6, 2018
- FDA recall number
- F-1771-2018 · event 80461
- Official record
- FDA enforcement report search
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