GIANT CURLY LEAF SPINACH, 12 /8 OZ, UPC: 6-88267-09813-0. Packaged in sealed plastic bags, 12 in a case.
Summary
The FDA issued a Class I for GIANT CURLY LEAF SPINACH, 12 /8 OZ, UPC: 6-88267-09813-0. Packaged in sealed pl by Lancaster Foods LLC. Reason: Possible contamination with listeria monocytogenes.
Details
Source
Food Recall
External ID
F-0922-2023
Action Date
2023-05-31
Status
Terminated
Category
food
Product Description
GIANT CURLY LEAF SPINACH, 12 /8 OZ, UPC: 6-88267-09813-0. Packaged in sealed plastic bags, 12 in a case.
Lot/Code Info: Best By April 29 2023
Quantity Affected: 486 cases
Reason for Recall
Possible contamination with listeria monocytogenes
Distribution
Distributors and retailers in MA, MD, PA, NY, NJ, and VA.
Type: Voluntary: Firm initiated
Recall Initiated: 2023-05-05
Company
Jessup, MD
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 71 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Lancaster Foods LLC has 4 FDA actions in our database, including 4 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 (Lancaster Foods LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Lancaster Foods LLC have FDA actions?
Lancaster Foods LLC has 4 FDA actions in our database, including 4 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0922-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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