Basil Pesto & Mozzarella Pizza NET WT. 13.90OZ (394g) UPC 8 57919 00785 5 Distributed by: Grocery Delivery E-Services Ne
Summary
The FDA issued a Class II for Basil Pesto & Mozzarella Pizza NET WT. 13.90OZ (394g) UPC 8 57919 00785 5 Distri by Bakkavor. Reason: Metal fragments in bread. The firm discovered metal fragments in various bread products. They determined the cause to be roasted tomatoes provided by .
Details
Source
Food Recall
External ID
H-0618-2026
Action Date
2026-04-01
Status
Ongoing
Category
food
Product Description
Basil Pesto & Mozzarella Pizza NET WT. 13.90OZ (394g) UPC 8 57919 00785 5 Distributed by: Grocery Delivery E-Services New York, NY 10005
Lot/Code Info: Hello Fresh Basil Pesto and Mozzarella Pizza: Lot 20367483 UB 6/29/26, Lot 20367483 UB 6/30/26, Lot 20377537 UB 9/4/26 & Lot 20377821 UB 9/5/26.
Quantity Affected: 2,337cs/15/13.9oz pkgs
Reason for Recall
Metal fragments in bread. The firm discovered metal fragments in various bread products. They determined the cause to be roasted tomatoes provided by one of their ingredient suppliers.
Distribution
Product was shipped to the following states: AZ, CA, CT, FL, IL, MI, NC, NJ, TX & VA.
Type: Voluntary: Firm initiated
Recall Initiated: 2026-01-19
Company
Charlotte, NC
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 64 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Bakkavor has 3 FDA actions in our database, including 3 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
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 (Bakkavor) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Bakkavor have FDA actions?
Bakkavor 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 "H-0618-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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