FDA recall record

Fisherman's Pride Processor, Inc. dba Neptune Schwan's Garlic Herb Shrimp NET WT 16 oz recall — FDA F-0130-2020

Product mis-packaging; causing undeclared allergens (milk and soy lecithin).

Class Iclassification
F-0130-2020official record ID
Nov 13, 2019report date

Recall record at a glance

Official recordF-0130-2020
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmFisherman's Pride Processor, Inc. dba Neptune Foods
Report dateNov 13, 2019
Recall initiation dateOct 8, 2019
Quantity1,872 individual sales units
LocationVernon, CA, United States

Official product description

Schwan's Garlic Herb Shrimp NET WT 16 oz. (1 lb.) Keep Frozen Cook Thoroughly Distributed By: Schwan's Home Service, Inc. Marshall. MN 56258 UPC 052008

Why the product was recalled

Product mis-packaging; causing undeclared allergens (milk and soy lecithin).

Distribution information

U.S. distribution to the following: MN No foreign distribution.

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly 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.