Buckhead Tuna
Reason The Firm was notified by NJ Department of Health of two samples collected from tuna with reported high levels of scombrotoxin.
Schwan's Garlic Herb Shrimp recall
Recalled by Fisherman's Pride Processor, Inc. dba Neptune Foods · Vernon, CA, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Product mis-packaging; causing undeclared allergens (milk and soy lecithin).
Undeclared allergens: Milk Soy
For someone with a food allergy the label is the only protection. An undeclared allergen can trigger a severe reaction even in a trace amount, which is why most of these recalls are Class I. All undeclared allergens recalls.
What was recalled
Schwan's Garlic Herb Shrimp NET WT 16 oz. (1 lb.) Keep Frozen Cook Thoroughly Distributed By: Schwan's Home Service, Inc. Marshall. MN 56258 UPC 052008
Quantity: 1,872 individual sales units
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.
Date code 4A924608xx-B1
Where it was sold
Minnesota
FDA's distribution note: U.S. distribution to the following: MN No foreign distribution.
Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. The risk from an undeclared allergen is to people allergic to milk, soy; for anyone else the product is generally not a safety concern. 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
- Fisherman's Pride Processor, Inc. dba Neptune Foods
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Oct 8, 2019
- In FDA report of
- Nov 13, 2019
- Terminated
- Dec 4, 2019
- FDA recall number
- F-0130-2020 · event 84024
- Official record
- FDA enforcement report search
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