Class IIOngoingVoluntary: Firm initiated

MAYEJ COMERCIALIZADORA S. de R.L. de C.V.: food recall H-0392-2026

MAYEJ COMERCIALIZADORA S. de R.L. de C.V. of Pueblo Acatzingo De Hidalgo recalled Italian Parsley packaged in 24lb boxes, 40 bunches per box in plastic. Reason: pathogen Cyclospora cayetanensis. The FDA listed it as Class II in its Enforcement Report dated Jan 14, 2026; distribution: nationwide.

Record status as published: Ongoing. openFDA data last updated Oct 21, 2026.

Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.

Recall details

Product
Italian Parsley packaged in 24lb boxes, 40 bunches per box in plastic.
Product quantity
1288 boxes
Reason for recall
pathogen Cyclospora cayetanensis
Codes, lots and dates on the package
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)
Distribution pattern
Nationwide
Recalling firm
MAYEJ COMERCIALIZADORA S. de R.L. de C.V., Pueblo Acatzingo De Hidalgo, Mexico
Classification
Class II — the FDA uses this class for a situation in which using or being exposed to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
Voluntary or mandated
Voluntary: Firm initiated
How the firm first notified customers
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Dates

EventDate
Recall initiated by the firmSep 26, 2025
Classified by the FDAJan 12, 2026
Published in the Enforcement ReportJan 14, 2026

All food recall records

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Sources

  • U.S. Food and Drug Administration, openFDA food enforcement reports, recall number H-0392-2026 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
  • Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service. The FDA does not endorse OpenPlate.