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Aldi Inc Recall: 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.

United States

TerminatedClass II

Company
Aldi Inc
Product
AnnaSea Wasabi Ahi Poke Hawaiian Poke Kits
Recall date
July 14, 2018
Terminated
October 5, 2018
Source
FDA

Reason for recall

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.

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
AnnaSea Wasabi Ahi Poke Hawaiian Poke Kits Not published in this source record Unknown Wasabi Ahi Hawaiian Poke Kit, UPC code 99221 0011 O. Products have best by dates of: 5/23/2020, 6/11/2020, 6/12/2020, and 6/14/2020.

Distribution

  • Domestic Only: NC
  • OH
  • MD
  • VA

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-1757-2018
Event ID
80551
Status
Terminated
Classification
Class II
Company
Aldi Inc
Product description
AnnaSea Wasabi Ahi Poke Hawaiian Poke Kits
Quantity
Unknown
Reason
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.
Recall initiation date
July 14, 2018
Report date
August 15, 2018
Classification date
Not published in this source record
Termination date
October 5, 2018
Distribution pattern
Domestic Only: NC, OH, MD, VA
UPC, lot, and code information
Wasabi Ahi Hawaiian Poke Kit, UPC code 99221 0011 O. Products have best by dates of: 5/23/2020, 6/11/2020, 6/12/2020, and 6/14/2020.
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
Press Release
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Other products recalled under this same event

This recall shares FDA event ID 80551 with 1 other product entry in Public Health Trace.

FDA Recall United States Terminated Historical recordClass II

Aldi Inc

Product
AnnaSea Limu Ahi Poke Hawaiian Poke Kits
Published
August 15, 2018
Distribution
Domestic Only: NC, OH, MD, VA

View recall →

Responsible company: Aldi Inc

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Distribution
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Published
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Distribution
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Product
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Published
November 14, 2018
Distribution
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Distribution map

A map highlighting the states named in the source's distribution description.

Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.

Distribution map
State Distributed
North Carolina 1
Ohio 1
Maryland 1
Virginia 1

States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace:

Frequently asked questions

What does a Class II mean?

A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.