Requeson (soft ricotta) 1 lb. packed into a clear clamshell package with no labeling information. "Requeson" is handwrit
Summary
The FDA issued a Class I for Requeson (soft ricotta) 1 lb. packed into a clear clamshell package with no labe by Nelson & Isa Lacteos LLC. Reason: Products may be contaminated with Listeria monocytogenes..
Details
Source
Food Recall
External ID
H-1189-2026
Action Date
2026-08-05
Status
Ongoing
Category
food
Product Description
Requeson (soft ricotta) 1 lb. packed into a clear clamshell package with no labeling information. "Requeson" is handwritten in black marker on the top lid of the clamshell package. No lot code or UPC.
Lot/Code Info: None
Quantity Affected: 480 (1-lb clamshell packages)
Reason for Recall
Products may be contaminated with Listeria monocytogenes.
Distribution
Only in NY.
Type: Voluntary: Firm initiated
Recall Initiated: 2026-06-05
Company
Bay Shore, NY
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 14 food recalls issued in the same week, part of 53 food-related FDA actions this month.
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 (Nelson & Isa Lacteos LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Nelson & Isa Lacteos LLC have FDA actions?
This is the only FDA action we have on record for Nelson & Isa Lacteos LLC in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-1189-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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