CLASS II Food recall · Reported 28 Jan 2026 · FDA Enforcement Report
Australian Greenlip Abalone, Frozen recalled
Southern Rocklobster LTD U is recalling Australian Greenlip Abalone, Frozen, distributed in California. The recall was initiated on 24 Dec 2025 and the FDA has classified it as Class II.
Check your package
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Recall details
- Recall number
- H-0406-2026
- FDA event ID
- 98229
- Recalling firm
- Southern Rocklobster LTD U, Vernon, CA
- Brand
- Australian Greenlip
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 24 Dec 2025
- FDA classified
- 16 Jan 2026
- Reported
- 28 Jan 2026
- Type
- Voluntary: Firm initiated
- Customers notified by
- Reason category
- Listeria
- Product category
- Other
Timeline
| 24 Dec 2025 | Recall initiated by company | |
| 16 Jan 2026 | Classified by FDA | +23 days |
| 28 Jan 2026 | Published in enforcement report | +12 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Potential Listeria Monocytogenes contamination
Listeria monocytogenes can grow at refrigerator temperatures. Infection is most dangerous for pregnant women, newborns, older adults and people with weakened immune systems. Symptoms can appear up to 70 days after eating contaminated food.
Product as listed by the FDA
Australian Greenlip Abalone, Frozen, 9 pieces, Net Wt. 23.5 OZ UPC: 9335533013342
Where it was distributed
Product was distributed to one customer in multiple locations throughout California.
Questions about this recall
Why was it recalled?
Potential Listeria Monocytogenes contamination
Which lots are affected?
Lot# 5996 Best Before: 29/11/2027
Where was it sold?
Product was distributed to one customer in multiple locations throughout California.
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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