RecallRadar
ModerateReported January 14, 2026

Italian Parsley packaged in 24lb boxes, 40 bunches per box in plastic.

Recalled by MAYEJ COMERCIALIZADORA S. de R.L. de C.V.

Food recall

MAYEJ COMERCIALIZADORA S. de R.L. de C.V.

Class II — moderate

Using this product might cause a temporary or medically reversible health problem. The chance of serious harm is low.

MAYEJ COMERCIALIZADORA S. de R.L. de C.V. has recalled Italian Parsley packaged in 24lb boxes, 40 bunches per box in plastic., according to data published by the U.S. Food and Drug Administration (FDA). The recall was reported on January 14, 2026 and was initiated on September 26, 2025. It is classified as a Class II recall, which means using this product might cause a temporary or medically reversible health problem. The chance of serious harm is low.

Below is a plain-English summary of what was recalled, why it was recalled, how to tell whether you have the affected product, and what steps you can take. For the complete and most current details, you can view the FDA record linked further down this page.

What was recalled?

This recall covers Italian Parsley packaged in 24lb boxes, 40 bunches per box in plastic., with approximately 1288 boxes affected. The company behind the recall is MAYEJ COMERCIALIZADORA S. de R.L. de C.V., based in Pueblo Acatzingo De Hidalgo. The FDA describes the product as: “Italian Parsley packaged in 24lb boxes, 40 bunches per box in plastic.”

Why was Italian Parsley packaged in 24lb boxes, 40 bunches per box in plastic. recalled?

According to the FDA, the stated reason for the recall is: “pathogen Cyclospora cayetanensis.”

What should you do?

If you think you may have bought Italian Parsley packaged in 24lb boxes, 40 bunches per box in plastic., compare it against the product description and identifying codes (Factura 154 - 75530 (1434328, 1434330, 1434330, 1434331, 1434332,1434333, 1434334. Factura 168 75613 (1436064, 1436065, 1436066, 1436067, 1436068, 1436069, 143…) before using it. This recall is currently listed as ongoing.

The general guidance for a matching product is to stop using it and follow the instructions in the official FDA recall notice, which may include a repair, replacement, refund, or safe disposal. When in doubt, contact MAYEJ COMERCIALIZADORA S. de R.L. de C.V. or your local health authority.

About this recall

This recall was distributed in Nationwide. RecallRadar summarizes recall information from public FDA data to make it easier to understand. We are an independent service and are not affiliated with the FDA or any government agency, so please always refer to the official source for the authoritative record — and note the “last synced” date shown on this page, since recall details can change over time.

Full recall details

Status
Ongoing
Date reported
January 14, 2026
Recall started
September 26, 2025
Distributed in
Nationwide
What was recalled
Italian Parsley packaged in 24lb boxes, 40 bunches per box in plastic.
Why it was recalled (as stated by the FDA)
pathogen Cyclospora cayetanensis
How to identify the affected product
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)
Amount recalled
1288 boxes

What you can do

Check whether any product you have matches the description and codes above. If it does, stop using it and follow the instructions in the official recall notice. When in doubt, contact the company or your local health authority.

Quick answers

Why was Italian Parsley packaged in 24lb boxes, 40 bunches per box in plastic. recalled?+

According to the FDA: pathogen Cyclospora cayetanensis

How serious is this recall?+

Class II — moderate. Using this product might cause a temporary or medically reversible health problem. The chance of serious harm is low.

What should I do if I have Italian Parsley packaged in 24lb boxes, 40 bunches per box in plastic.?+

Compare your product against the description and identifying codes on this page. If it matches, stop using it and follow the instructions in the official recall notice — this usually means returning it for a refund or discarding it. When in doubt, contact the company or your local health authority.

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View the official FDA record

Opens the U.S. Food and Drug Administration (FDA) data for this recall.

Recall number: H-0392-2026. Information last synced from the FDA on July 6, 2026.