RecallRadar
ModerateReported January 28, 2026

Australian Greenlip Abalone, Frozen, 9 pieces

Recalled by Southern Rocklobster LTD USA

Food recall

Southern Rocklobster LTD USA

Class II — moderate

Using this product might cause a temporary or medically reversible health problem. The chance of serious harm is low.

See all recalls involving Listeria

Southern Rocklobster LTD USA has recalled Australian Greenlip Abalone, Frozen, 9 pieces, according to data published by the U.S. Food and Drug Administration (FDA). The recall was reported on January 28, 2026 and was initiated on December 24, 2025. It is classified as a Class II recall, which means using this product might cause a temporary or medically reversible health problem. The chance of serious harm is low.

Below is a plain-English summary of what was recalled, why it was recalled, how to tell whether you have the affected product, and what steps you can take. For the complete and most current details, you can view the FDA record linked further down this page.

What was recalled?

This recall covers Australian Greenlip Abalone, Frozen, 9 pieces, with approximately 94 cases affected. The company behind the recall is Southern Rocklobster LTD USA, based in Vernon, CA. The FDA describes the product as: “Australian Greenlip Abalone, Frozen, 9 pieces, Net Wt. 23.5 OZ UPC: 9335533013342”

Why was Australian Greenlip Abalone, Frozen, 9 pieces recalled?

According to the FDA, the stated reason for the recall is: “Potential Listeria Monocytogenes contamination.” In plain terms, this recall relates to Listeria.

Listeria monocytogenes is a bacterium that can grow even at refrigerator temperatures, which makes it a particular concern in ready-to-eat foods. Health authorities warn that it can cause a serious infection called listeriosis, and that pregnant people, newborns, older adults, and those with weakened immune systems are especially vulnerable. This is why products potentially contaminated with Listeria are often recalled quickly.

What should you do?

If you think you may have bought Australian Greenlip Abalone, Frozen, 9 pieces, compare it against the product description and identifying codes (Lot# 5996 Best Before: 29/11/2027) before using it. This recall is currently listed as ongoing.

The general guidance for a matching product is to stop using it and follow the instructions in the official FDA recall notice, which may include a repair, replacement, refund, or safe disposal. When in doubt, contact Southern Rocklobster LTD USA or your local health authority.

About this recall

This recall was distributed in CA. RecallRadar summarizes recall information from public FDA data to make it easier to understand. We are an independent service and are not affiliated with the FDA or any government agency, so please always refer to the official source for the authoritative record — and note the “last synced” date shown on this page, since recall details can change over time.

Full recall details

Status
Ongoing
Date reported
January 28, 2026
Recall started
December 24, 2025
Distributed in
CA
What was recalled
Australian Greenlip Abalone, Frozen, 9 pieces, Net Wt. 23.5 OZ UPC: 9335533013342
Why it was recalled (as stated by the FDA)
Potential Listeria Monocytogenes contamination
How to identify the affected product
Lot# 5996 Best Before: 29/11/2027
Amount recalled
94 cases

What you can do

Check whether any product you have matches the description and codes above. If it does, stop using it and follow the instructions in the official recall notice. When in doubt, contact the company or your local health authority.

Quick answers

Why was Australian Greenlip Abalone, Frozen, 9 pieces recalled?+

According to the FDA: Potential Listeria Monocytogenes contamination

How serious is this recall?+

Class II — moderate. Using this product might cause a temporary or medically reversible health problem. The chance of serious harm is low.

What should I do if I have Australian Greenlip Abalone, Frozen, 9 pieces?+

Compare your product against the description and identifying codes on this page. If it matches, stop using it and follow the instructions in the official recall notice — this usually means returning it for a refund or discarding it. When in doubt, contact the company or your local health authority.

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View the official FDA record

Opens the U.S. Food and Drug Administration (FDA) data for this recall.

Recall number: H-0406-2026. Information last synced from the FDA on July 5, 2026.

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