Australian Greenlip Abalone, Frozen, 9 pieces, Net Wt. 23.5 OZ UPC: 9335533013342
Summary
The FDA issued a Class II for Australian Greenlip Abalone, Frozen, 9 pieces, Net Wt. 23.5 OZ UPC: 93355330133 by Southern Rocklobster LTD USA. Reason: Potential Listeria Monocytogenes contamination.
Details
Source
Food Recall
External ID
H-0406-2026
Action Date
2026-01-28
Status
Ongoing
Category
food
Product Description
Australian Greenlip Abalone, Frozen, 9 pieces, Net Wt. 23.5 OZ UPC: 9335533013342
Lot/Code Info: Lot# 5996 Best Before: 29/11/2027
Quantity Affected: 94 cases
Reason for Recall
Potential Listeria Monocytogenes contamination
Distribution
Product was distributed to one customer in multiple locations throughout California.
Type: Voluntary: Firm initiated
Recall Initiated: 2025-12-24
Company
Vernon, CA
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 32 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Southern Rocklobster LTD USA) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Southern Rocklobster LTD USA have FDA actions?
This is the only FDA action we have on record for Southern Rocklobster LTD USA in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0406-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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