Data Foundry

Food recalls 2019

5-pound cans of unpasteurized — Class I food recall F-0841-2019

Terminated recall by Bornstein Seafoods Inc, reported 2019-02-13, distributed in CA, OR. 5-pound cans of unpasteurized, reduced oxygen packaged (ROP), ready-to-eat, Dungeness crab meat are recalled b

Recall numberF-0841-2019
Product typeFood
ClassificationClass I
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmBornstein Seafoods Inc, Bellingham, WA, United States
Recall initiated2018-12-21
Classified2019-02-06
Reported by FDA2019-02-13
Terminated2019-07-05
DistributedCA, OR
Quantity1,715 pounds
Reason classesmicrobial contamination, temperature control
Pathogensclostridium botulinum
Lot numbersA11739, A11759

Product

5-pound cans of unpasteurized, ready-to-eat, Dungeness crab meat, packaged in reduced oxygen metal cans that were shipped with Fresh-Check B Time Temperature Indicator (TTIs). Product was shipped frozen. The label is read in parts: "***BORNSTEIN SEAFOODS ***WILD Dungeness CRAB MEAT***INGREDIENTS: CRAB MEAT WITH SALT ADDED ***NET WT 5 LB***HANDLING INSTRUCTIONS: To protect the delicate flavor and texture of this crab meat, we recommend the following handling practices***KEEP REFRIGERATED: 33-38 degrees F, after opening, cover remaining product during storage***PACKED BY BORNSTEIN SEAFOODS INC. ASTORIA, OR 97103***".

Reason for recall

5-pound cans of unpasteurized, reduced oxygen packaged (ROP), ready-to-eat, Dungeness crab meat are recalled because the incorrect Time Temperature Indicator (TTI) was applied to the cans. The TTI would not indicate the temperature abuse. If the product was temperature abused, it would create the potential hazard of Clostridium botulinum growth and toxin formation.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/F-0841-2019. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.