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Banks Square Market Corp dba The Produce Connection Recall: Product may be contaminated with Listeria monocytogenes. - F-1960-2018

United States

TerminatedClass II

Company
Banks Square Market Corp dba The Produce Connection
Product
Zuchini noodles packaged under the following brands - the PI…
Recall date
August 6, 2018
Terminated
September 27, 2018
Source
FDA

Reason for recall

Product may be contaminated with Listeria monocytogenes.

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
Zuchini noodles packaged under the following brands - the PICK, NET WT 16 OZ, UPC: 8 54340 00700 3; Whole Foods, UPC: 0 36406 30488 6 Not published in this source record 2,727 cases (total for all products) All lots within expiry.

Distribution

  • Product was directly distributed to the following states: MA
  • MD
  • NY

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-1960-2018
Event ID
80732
Status
Terminated
Classification
Class II
Company
Banks Square Market Corp dba The Produce Connection
Product description
Zuchini noodles packaged under the following brands - the PICK, NET WT 16 OZ, UPC: 8 54340 00700 3; Whole Foods, UPC: 0 36406 30488 6
Quantity
2,727 cases (total for all products)
Reason
Product may be contaminated with Listeria monocytogenes.
Recall initiation date
August 6, 2018
Report date
August 29, 2018
Classification date
Not published in this source record
Termination date
September 27, 2018
Distribution pattern
Product was directly distributed to the following states: MA, MD, NY
UPC, lot, and code information
All lots within expiry.
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Other products recalled under this same event

This recall shares FDA event ID 80732 with 2 other product entries in Public Health Trace.

FDA Recall United States TerminatedTerminated: September 27, 2018Historical recordClass II

Banks Square Market Corp dba The Produce Connection

Product
Zuchini and summer squash mixed noodles packaged under the f…
Published
August 29, 2018
Distribution
Product was directly distributed to the…

View recall →

FDA Recall United States TerminatedTerminated: September 27, 2018Historical recordClass II

Banks Square Market Corp dba The Produce Connection

Product
Summer squash noodles packaged under the following brands -…
Published
August 29, 2018
Distribution
Product was directly distributed to the…

View recall →

Responsible company: Banks Square Market Corp dba The Produce Connection

Other recalls from Banks Square Market Corp dba The Produce Connection

FDA Recall United States TerminatedTerminated: September 27, 2018Historical recordClass II

Banks Square Market Corp dba The Produce Connection

Product
Zuchini and summer squash mixed noodles packaged under the f…
Published
August 29, 2018
Distribution
Product was directly distributed to the…

View recall →

FDA Recall United States TerminatedTerminated: September 27, 2018Historical recordClass II

Banks Square Market Corp dba The Produce Connection

Product
Summer squash noodles packaged under the following brands -…
Published
August 29, 2018
Distribution
Product was directly distributed to the…

View recall →

Distribution map

A map highlighting the states named in the source's distribution description.

Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.

Distribution map
State Distributed
Massachusetts 1
Maryland 1
New York 1

States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information. See FDA Enforcement Reports versus recall announcements for how that database differs from a press-release-style announcement.

New to reading a recall record? See how to read an FDA recall record and what recall statuses mean.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace:

Frequently asked questions

What does a Class II mean?

FDA classifies this recall as Class II. See how to read an FDA recall record (linked above) for what each classification level means.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the responsible agency's published instructions, linked below -- recall guidance is set by that agency, not by Public Health Trace.

Official guidance and record verification

Public Health Trace does not provide medical advice -- review the linked official source below for current, authoritative information.

How to interpret this historical record

This record is preserved as published by FDA, as of September 27, 2018.

Status as reported: Terminated.

This page does not imply a current danger or a current consumer instruction -- review the official source for the most current information.

View the official FDA source

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.

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