Orchids brand Whole Oysters
Reason The product has been prepared, packed, or held under insanitary conditions whereby it may have become contaminated with filth, or whereby it may have been rendered injurious to health.
Orchids brand Smoked Oysters in cottonseed oil recall
Recalled by CTC Food International Inc · South San Francisco, CA, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
The product has been prepared, packed, or held under insanitary conditions whereby it may have become contaminated with filth, or whereby it may have been rendered injurious to health.
These are failures of the safety steps that keep food safe - cooking, pasteurising, keeping cold, sealing - even when no contaminant has yet been found. All processing & sanitation problems recalls.
What was recalled
Orchids brand Smoked Oysters in cottonseed oil, salt added. Net Wt. 3 oz Ingredients: oysters, salt, water. Packed for CTC Food Int'l Inc. South San Francisco, CA 94080 Product of Korea
Quantity: 797 cases (25 x 3 oz)
Food: Seafood & fish
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
UPC 0 74601 00090 5; all codes
Where it was sold
California
FDA's distribution note: California only
Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- CTC Food International Inc
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Jun 1, 2012
- In FDA report of
- Jun 20, 2012
- Terminated
- Feb 12, 2013
- FDA recall number
- F-1436-2012 · event 62022
- Official record
- FDA enforcement report search
Also recalled with it (1 more product)
FDA files each product of one recall action separately; these share the same FDA event.
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