FDA recall record

Aldi AnnaSea Limu Ahi Poke Hawaiian Poke Kits recall — FDA F-1758-2018

ALDI has voluntarily recalled AnnaSea Wasabi Ahi Poke Hawaiian Poke Kits and Limu Ahi Poke Hawaiian Poke Kits due to storing the products at temperatures…

Class IIclassification
F-1758-2018official record ID
Aug 15, 2018report date

Recall record at a glance

Official recordF-1758-2018
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmAldi Inc.
Report dateAug 15, 2018
Recall initiation dateJul 14, 2018
QuantityUnknown
LocationBatavia, IL, United States

Official product description

AnnaSea Limu Ahi Poke Hawaiian Poke Kits

Why the product was recalled

ALDI has voluntarily recalled AnnaSea Wasabi Ahi Poke Hawaiian Poke Kits and Limu Ahi Poke Hawaiian Poke Kits due to storing the products at temperatures above freezing prior to consumption which can render the products unsafe for consumption.

Distribution information

Domestic Only: NC, OH, MD, VA

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Press Release.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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