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FDA recall H-0406-2026 · Jan 28, 2026

Southern Rocklobster LTD USA: Australian Greenlip Abalone recall

Product

Australian Greenlip Abalone, Frozen, 9 pieces, Net Wt. 23.5 OZ UPC: 9335533013342

Reason for recall

Potential Listeria Monocytogenes contamination

What to do

FDA enforcement reports don't include consumer instructions. Check the codes below against your package, and look for the company's notice on FDA's recalls page. If you have the product and aren't sure, don't use it until you've checked.

Recall details

FDA classification
Class II: use of or exposure to the product may cause temporary or medically reversible health problems, or the chance of serious problems is remote.
Status
Terminated
Codes, lots and dates
Lot# 5996 Best Before: 29/11/2027
Quantity
94 cases
Distribution
Product was distributed to one customer in multiple locations throughout California.
Recalling firm
Southern Rocklobster LTD USA, Vernon, CA
Voluntary or mandated
Voluntary: Firm initiated
Recall started
2025-12-24

Source: openFDA enforcement record H-0406-2026 · search recall number H-0406-2026 in FDA's Enforcement Report.

Copied from the agency record without changes. Data as of Oct 14, 2026, 1:15 AM EDT. The agency notice is the final word.

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