A-PAC Farm Raised Shrimp
Reason Salmonella detected in product
A-PAC Farm Raised Shrimp recall
Recalled by Censea Inc · Northbrook, IL, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Salmonella detected in product
Pathogen: Salmonella
Salmonella is the most common cause of food recalls for bacteria, often in eggs, produce, nuts and spices.
The most serious food recalls: a contaminated product can cause outbreaks, hospitalisations and deaths, especially for pregnant people, young children, older adults and anyone with a weakened immune system. All bacteria & viruses recalls.
What was recalled
A-PAC Farm Raised Shrimp, A Product of Vietnam, Keep Frozen At 0 Degrees F (-18 Degrees Celsius), Net Weight 4 lbs (64 oz). Above UPC Code: APAC 4/6 ct Headless Tiger Shrimp
Quantity: 6 cases
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.
Lot 38452NK
Where it was sold
Connecticut Illinois Kentucky Massachusetts New Jersey New York Rhode Island Texas Virginia
FDA's distribution note: NY, NJ, RI, MA, TX, IL, CT, VA, KY
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. 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
- Censea Inc
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Sep 9, 2016
- In FDA report of
- Dec 21, 2016
- Terminated
- Jul 17, 2019
- FDA recall number
- F-0739-2017 · event 75180
- 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.
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Reason Product tested positive for Salmonella
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