CLASS II Food recall · Reported 29 Aug 2012 · FDA Enforcement Report
Oysters, Frozen IQF recalled by LD Amory &
LD Amory is recalling Oysters, Frozen IQF, distributed in Arizona, North Carolina, Virginia. The recall was initiated on 15 May 2012 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
- F-1950-2012
- FDA event ID
- 62623
- Recalling firm
- LD Amory, Hampton, VA
- Brand
- Oysters
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 15 May 2012
- FDA classified
- 20 Aug 2012
- Reported
- 29 Aug 2012
- Type
- Voluntary: Firm initiated
- Customers notified by
- Telephone
- Reason category
- Norovirus
- Product category
- Oysters & Shellfish
Timeline
| 15 May 2012 | Recall initiated by company | |
| 20 Aug 2012 | Classified by FDA | +97 days |
| 29 Aug 2012 | Published in enforcement report | +9 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Molluscan shellfish may have been exposed to human fecal waste and are potentially contaminated with norovirus.
Product as listed by the FDA
Oysters, Frozen IQF, packaged in 5 lb bags, 6x5 lb/cartons, labeled in part ***Product of Korea***
Where it was distributed
The products were distributed to AZ, NC, and VA.
Questions about this recall
Why was it recalled?
Molluscan shellfish may have been exposed to human fecal waste and are potentially contaminated with norovirus.
Which lots are affected?
All codes
Where was it sold?
The products were distributed to AZ, NC, and VA.
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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