FDA recall record

Hahn, Harry O Seafood Gold Label Shrimp Dip in 7 oz plastic containers, Manufactured recall — FDA F-1354-2014

Red #40 color additive in shrimp raw ingredient undeclared on finished product label of various shrimp dips and salads.

Class IIIclassification
F-1354-2014official record ID
Jan 8, 2014report date

Recall record at a glance

Official recordF-1354-2014
CategoryFood Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmHahn, Harry O Seafood Inc.
Report dateJan 8, 2014
Recall initiation dateSep 5, 2013
Quantity89.25lbs
LocationWest Lawn, PA, United States

Official product description

Gold Label Shrimp Dip in 7 oz plastic containers, Manufactured by Adelphia Seafood, ingredients: cream cheese (pasteurized milk & cream, cheese culture, salt, stabilizers (carob bean and/or xanthan gums), water, shrimp, surimi (fish protein (pollock, cod and/or pacific whiting), water, wheat/corn starch, natural crab extract, soy oil), shrimp base (shrimp, salt, monosodium glutamate, spices), contains 2% or less of the following: spices, natural preservative (inactive dry yeast, lactic acid, cultured dextrose, maltodextrin, sodium diacetate, egg white lysozyme, nisin preparation) Allergens: milk, fish, crustacean shellfish, egg, wheat, soy.

Why the product was recalled

Red #40 color additive in shrimp raw ingredient undeclared on finished product label of various shrimp dips and salads.

Distribution information

PA, MD.

How to read the classification

FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Telephone.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.

Related recall records

Other records from the same recalling company are shown first when available.