RecallHawk
Class II Recall

Buurma Farms Plain Parsley (Flat Parsley) PLU twist tie or banded bunches 30ct in cardboard cartons 60ct in wooden crate

Buurma Farms Inc

Summary

The FDA issued a Class II for Buurma Farms Plain Parsley (Flat Parsley) PLU twist tie or banded bunches 30ct i by Buurma Farms Inc. Reason: Potentially contaminated with E. Coli.

Details

Source

Food Recall

External ID

F-0014-2022

Action Date

2021-10-20

Status

Terminated

Category

food

Product Description

Buurma Farms Plain Parsley (Flat Parsley) PLU twist tie or banded bunches 30ct in cardboard cartons 60ct in wooden crates

Lot/Code Info: UPC 3338380125 Harvest Lot 2A242A6 Lot Numbers: GTIN(01)00032958701050(10)2B243A6 Product Numbers: PLU4901

Quantity Affected: 315 Total

Reason for Recall

Potentially contaminated with E. Coli

Distribution

MI, OH, IL, NY, SC, PA

Type: Voluntary: Firm initiated

Recall Initiated: 2021-09-13

Company

Buurma Farms Inc

Willard, OH

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 17 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 (Buurma Farms Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Buurma Farms Inc have FDA actions?

This is the only FDA action we have on record for Buurma Farms Inc in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0014-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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