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U.S. Department of Health and Human Services

Medical Devices

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Complications Related to the Use of Vascular Hemostasis Devices

This is an archived document and is no longer current information.

October 8, 1999


Dear Colleague:

I am writing to inform you of adverse events related to the use of vascular hemostasis devices. These devices provide an alternative to manual compression in achieving hemostasis following percutaneous femoral arterial punctures in patients undergoing diagnosis and treatment for cardiovascular disease. Reported complications related to these devices include hematoma, retroperitoneal bleed, pseudoaneurysm, late bleeding, and infrequently, death.



Since 1996, FDA has received reports of adverse events, including deaths, concerning closure devices. In one case, a patient, who had previously been treated with a vascular hemostasis device, suffered an acute myocardial infarction. During the ensuing catheterization, the hemostasis device was dislodged, necessitating surgical intervention. In another case, following closure with a vascular hemostasis device, the patient was discharged only to return days later with bleeding from the groin. This patient then required surgery to repair a ruptured pseudoaneurysm.

Complications can also occur when manual compression is used to achieve hemostasis. Review of the literature does show that the types of complications associated with manual compression and vascular hemostasis devices are similar. After analyzing the specific circumstances that led to the adverse events reported for vascular hemostasis devices, we believe that the following recommendations may be helpful in minimizing adverse events relating to the use of these devices.



Manufacturers’ instructions and recommendations may vary for individual vascular hemostasis devices. In general, to avoid complications when using vascular hemostasis devices, we recommend that you carefully follow the device manufacturer’s warnings, precautions, and instructions regarding patient selection and device use.

In addition, we offer the following specific recommendations:

  • Do not use vascular hemostasis devices to treat patients with suspected double wall punctures, as punctures of the posterior wall are not closed with these devices.
  • Carefully weigh the risk of bleeding at the puncture site against the benefits of using a vascular hemostasis device when treating patients with bleeding disorders or patients medicated with platelet glycoprotein IIb/IIIa receptor inhibitors.
  • Carefully monitor the groin puncture site to minimize the occurrence of complications with vascular hemostasis devices.
  • Special attention should be paid to any post-procedure patient-management instructions or ambulation recommendations for the specific vascular hemostasis device used.


Reporting adverse events to FDA

FDA is interested in additional data on adverse events involving the use of hemostasis devices. Healthcare providers employed by facilities that are subject to FDA’s user facility reporting requirements should follow the reporting procedures established by their facility. All other providers may submit their reports to MedWatch, FDA’s voluntary reporting program. The reports can be submitted by phone at 1-800-FDA-1088; by fax at 1-800-FDA-0178; via the MedWatch web site; or by mail to MedWatch, FDA, HF-2, 5600 Fishers Lane, Rockville, Maryland 20852-9787.


Getting more information

If you have questions about this Notification, please contact FDA's  Division of of Small Manufacturers, International and Consumer Assistance (DSMICA) by e-mail at dsmica@fda.hhs.gov or by phone at 1-800-638-2041 or 301-796-7100

FDA Medical Device Public Health Notifications are available on the Internet. You can also be notified through email each time a new Public Health Notification is added to our web page. To subscribe, visit: http://service.govdelivery.com/service/subscribe.html?code=USFDA_39.

Sincerely yours, 

David W. Feigal, Jr., M.D., M.P.H
Center for Devices and Radiological Health
Food and Drug Administration