Scarpetta brand Pink Pesto Pasta Sauce; INGREDIENTS: Tomatoes (tomatoes, tomato juice, citric acid), Cream, Onions, Oliv
Summary
The FDA issued a Class I for Scarpetta brand Pink Pesto Pasta Sauce; INGREDIENTS: Tomatoes (tomatoes, tomato by BC Gourmet USA, Inc.. Reason: Product contains undeclared pine nuts..
Details
Source
Food Recall
External ID
F-0771-2023
Action Date
2023-05-10
Status
Terminated
Category
food
Product Description
Scarpetta brand Pink Pesto Pasta Sauce; INGREDIENTS: Tomatoes (tomatoes, tomato juice, citric acid), Cream, Onions, Olive Oil, Basil, Garlic, Salt, Black Pepper, Citric Acid.; CONTAINS: MILK.; BC Gourmet USA, Inc., Lynn, MA;
Lot/Code Info: Lot Code NN149 Expiration date 5/2/2023 Lot Code NN164 Expiration date 12/9/2023
Quantity Affected: 906 units
Reason for Recall
Product contains undeclared pine nuts.
Distribution
NJ, PA, MA
Type: Voluntary: Firm initiated
Recall Initiated: 2023-03-14
Company
Lynn, MA
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 65 food recalls issued in the same week, part of 204 food-related FDA actions this month.
BC Gourmet USA, Inc. has 3 FDA actions in our database, including 3 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 (BC Gourmet USA, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does BC Gourmet USA, Inc. have FDA actions?
BC Gourmet USA, Inc. has 3 FDA actions in our database, including 3 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0771-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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