Class IIITerminated in FDA datasetRecall initiated Sep 5, 2013

Adelphia Seafood Shrimp & Scallop Rotini, in 5 lb. plastic tubs, Adelphia Seafood, West Lawn,…

Recalling firm: Hahn, Harry O Seafood Inc

Why it was recalled

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

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Oct 20, 2014.

Check your package

Compare the exact product and package details with the label you have.

ProductAdelphia Seafood Shrimp & Scallop Rotini, in 5 lb. plastic tubs, Adelphia Seafood, West Lawn, PA. Ingredients: pasta, oil (soybean and olive), cider vinegar, water, shrimp, scallops, red & green peppers, red onion, food starch, salt, spices, natural preservatives. Allergens: soybeans, shellfish, wheat
Package size5 lb

FDA code information

Use by 9/21/13

Match the product, package size, and code together. A missing match does not guarantee safety.

Full FDA record and distribution details

Original product description

Adelphia Seafood Shrimp & Scallop Rotini, in 5 lb. plastic tubs, Adelphia Seafood, West Lawn, PA. Ingredients: pasta, oil (soybean and olive), cider vinegar, water, shrimp, scallops, red & green peppers, red onion, food starch, salt, spices, natural preservatives. Allergens: soybeans, shellfish, wheat

Original FDA recall reason

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

Recall details

Recall number
F-1356-2014
Event ID
66292
FDA status
Terminated
Initiated
Sep 5, 2013
Reported
Jan 8, 2014
Classified
Jan 2, 2014
Terminated
Oct 20, 2014
Quantity
30 lbs
Location
West Lawn, PA, United States
Initiation type
Voluntary: Firm initiated
Notification
Telephone

Where it was distributed

PA, MD.

FDA source record · F-1356-2014

Data updated September 16, 2026. View official FDA data ↗

Follow official FDA and manufacturer guidance.