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  4. Cook Medical Issues Voluntary Recall of Transseptal Needle and Transseptal Needle with Catheter
  1. Recalls, Market Withdrawals, & Safety Alerts

COMPANY ANNOUNCEMENT

Cook Medical Issues Voluntary Recall of Transseptal Needle and Transseptal Needle with Catheter

This recall has been completed and FDA has terminated this recall.

When a company announces a recall, market withdrawal, or safety alert, the FDA posts the company's announcement as a public service. FDA does not endorse either the product or the company.

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Summary

Company Announcement Date:
FDA Publish Date:
Product Type:
Medical Devices
Reason for Announcement:
Recall Reason Description
Complaints of rust on the products
Company Name:
Cook Medical
Brand Name:
Brand Name(s)
Cook Medical
Product Description:
Product Description
Transseptal Needle and Transseptal Needle Catheter

Company Announcement

Bloomington, Ind. — On October 8, 2021, Cook Medical issued a global, voluntary recall of the Transseptal Needle and the Transseptal Needle with Catheter. This recall includes all unexpired lots for both of these products. The needles were recalled due to complaints of rust on the products. Use of affected products could result in increased procedural time and inflammatory reactions, including systemic reactions which may lead to permanent impairment or death.

The U.S. Food and Drug Administration (FDA) has not yet classified the recall. A complete list of products affected by this recall can be found below.

Transseptal Needles, including Transseptal Needles with Catheters, were found to have rust internally, externally, or both. To date, Cook Medical has received no reports of injury or illness related to this recall. Cook has received four complaints where the presence of rust was identified prior to patient contact. However, please be advised that the presence of rust may go undetected by the user. The FDA and other regulatory agencies around the world have been notified of this action.

Potential adverse events

If an affected product is used, potential negative outcomes include increased procedural time (to obtain a replacement device) and inflammatory reactions ranging from local or self-limited reactions to systemic reactions requiring medical intervention. Systemic reactions could potentially lead to permanent impairment or death.

Affected products

PRODUCT
BRAND NAME

INTENDED USE

REFERENCE PART NUMBER (RPN)

ORDER NUMBER (GPN)

LOT NUMBER / UDI

RANGE OF MANUFACTURE DATES FOR AFFECTED PRODUCTS

Transseptal Needle Intended for transseptal left heart access in both diagnostic and interventional procedures TSNC-18-71.0 G02364 All October 02, 2016 through July 22, 2021
TSNC-19-56.0 G02365
Transseptal Needle with Catheter Intended to facilitate transseptal entry into the left atrium TSN-17-75.0-ENDRYS G19261

Recall return information

Customers that received products affected by the recall were sent prepaid labels in a recall information packet. The letters requested that all customers and distributors quarantine and discontinue use of all potentially affected units and return the affected products to Cook as soon as possible for credit.

Customers in the U.S. and in Latin America should return affected product(s) to Cook Medical. Before returning affected product to Cook Medical, please obtain an RGA#. You may contact 800.457.4500, press option 5, and enter extension 151090 to obtain an RGA# and return address.

Adverse event reporting

Report adverse events to Cook Medical Customer Relations. Adverse events or quality problems experienced with the use of this product may also be reported to the FDA’s MedWatch Adverse Event Reporting program either online, by regular mail, or by fax.

Cook Medical Customer Service
Phone: 1.800.457.4500 or 1.812.339.2235, Monday – Friday between 7:30 am – 5:00 pm (EST)
Email: CustomerRelationsNA@cookmedical.com
U.S. Food and Drug Administration
Phone: 1.800.FDA.1088
Web: http://www.fda.gov/Safety/MedWatch/HowToReport/default.htm

FDA MedWatch Adverse Event Reporting
Regular Mail or Fax: Download form or call 1- 800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178

About Cook Medical
Since 1963, Cook Medical has worked closely with physicians to develop technologies that eliminate the need for open surgery. Today we invent, manufacture and deliver a unique portfolio of medical devices to the healthcare systems of the world. Serving patients is a privilege, and we demand the highest standards of quality, ethics and service. We have remained family owned so that we have the freedom to focus on what we care about: patients, our employees and our communities.

Find out more at CookMedical.com and for the latest news, follow us on Twitter, Facebook and LinkedIn.


Company Contact Information

Consumers:
Cook Medical Customer Service
1.800.457.4500 or 1.812.339.2235
CustomerRelationsNA@cookmedical.com

Product Photos

 
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