Fresh Salmon Deep Skin Fillets packed in 10-50 lb. corrugated cardboard or Styrofoam boxes
Summary
The FDA issued a Class I for Fresh Salmon Deep Skin Fillets packed in 10-50 lb. corrugated cardboard or Styro by Mariscos Bahia Inc. Reason: Possible contamination with salmonella.
Details
Source
Food Recall
External ID
F-0089-2023
Action Date
2022-11-09
Status
Terminated
Category
food
Product Description
Fresh Salmon Deep Skin Fillets packed in 10-50 lb. corrugated cardboard or Styrofoam boxes
Lot/Code Info: Product Code: SALFDS
Quantity Affected: 40,338.15 lbs
Reason for Recall
Possible contamination with salmonella
Distribution
Product was distributed to 179 customers located in Arizona and California. The firm utilizes 3 distributors in California and 2 in Arizona. End users are primarily restaurants.
Type: Voluntary: Firm initiated
Recall Initiated: 2022-10-20
Company
Pico Rivera, CA
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 58 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Mariscos Bahia Inc has 7 FDA actions in our database, including 7 recalls.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Mariscos Bahia Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Mariscos Bahia Inc have FDA actions?
Mariscos Bahia Inc has 7 FDA actions in our database, including 7 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0089-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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