Buckhead Tuna
Reason The Firm was notified by NJ Department of Health of two samples collected from tuna with reported high levels of scombrotoxin.
THE ORIGINAL SOUPMAN Lobster Bisque recall
Recalled by Original Soup Man · Staten Island, NY, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
The Original Soup Man has recalled Lobster Bisque due to the presense of Undeclared Shrimp, Tilapia and Perch.
Undeclared allergen: Shellfish
For someone with a food allergy the label is the only protection. An undeclared allergen can trigger a severe reaction even in a trace amount, which is why most of these recalls are Class I. All undeclared allergens recalls.
What was recalled
THE ORIGINAL SOUPMAN Lobster Bisque, Net Wt 17 oz (482 g). Product is packed as a tetra pak and ships as a pack of 12 or 6 containers per carton. Distributed exclusively by: SoupMan Inc. Staten Island, NY 10314
Quantity: Total of 3,083 cases (1859 cases/12/17 oz and 1244 cases/6/17 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.
Lot numbers: 0314435801, 0411435801, 0523435801, 0709435803, 0822435801, 0709435802 and 0821435801
Where it was sold
Nationwide.
FDA's distribution note: retail stores nationwide
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. The risk from an undeclared allergen is to people allergic to shellfish; for anyone else the product is generally not a safety concern. 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
- Original Soup Man
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Sep 24, 2014
- In FDA report of
- Nov 26, 2014
- Terminated
- May 3, 2017
- FDA recall number
- F-0504-2015 · event 69297
- Official record
- FDA enforcement report search
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