Italian Parsley packaged in 24lb boxes, 40 bunches per box in plastic.
Summary
The FDA issued a Class II for Italian Parsley packaged in 24lb boxes, 40 bunches per box in plastic. by MAYEJ COMERCIALIZADORA S. de R.L. de C.V.. Reason: pathogen Cyclospora cayetanensis.
Details
Source
Food Recall
External ID
H-0392-2026
Action Date
2026-01-14
Status
Ongoing
Category
food
Product Description
Italian Parsley packaged in 24lb boxes, 40 bunches per box in plastic.
Lot/Code Info: Factura 154 - 75530 (1434328, 1434330, 1434330, 1434331, 1434332,1434333, 1434334. Factura 168 75613 (1436064, 1436065, 1436066, 1436067, 1436068, 1436069, 1436070, 1436071) Factura 177 75700 (1437701, 1437702, 1437703, 1437704, 1437705, 1437706, 1437707, 1737708)
Quantity Affected: 1288 boxes
Reason for Recall
pathogen Cyclospora cayetanensis
Distribution
Nationwide
Type: Voluntary: Firm initiated
Recall Initiated: 2025-09-26
Company
Pueblo Acatzingo De Hidalgo
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 36 food recalls issued in the same week, part of 204 food-related FDA actions this month.
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 (MAYEJ COMERCIALIZADORA S. de R.L. de C.V.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does MAYEJ COMERCIALIZADORA S. de R.L. de C.V. have FDA actions?
This is the only FDA action we have on record for MAYEJ COMERCIALIZADORA S. de R.L. de C.V. in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0392-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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