Contact Us

Defective Medical Devices
*    Denotes required field.

   * First Name 

   * Last Name 

   * Email 


Cell Phone 

Street Address 

Zip Code 



Date when device was implanted :

Please describe any problems or injuries caused by the product:

For verification purposes, please answer the below question:

No Yes, I agree to the Parker Waichman LLP disclaimers. Click here to review.

Yes, I would like to receive the Parker Waichman LLP monthly newsletter, InjuryAlert.

please do not fill out the field below.

FDA seizes flawed infusion pumps from Cardinal

Aug 28, 2006 | The Food and Drug Administration seized infusion pumps made by a unit of Cardinal Health, Dublin, Ohio, and the company said it was suspending installation, production, sale and repair of the pumps. Earlier this month, Cardinal's Alaris Products unit, which makes the pumps, issued an urgent recall notice to customers, warning that the pumps' keypads could register numbers twice and lead to overdoses. Alaris advised healthcare facilities on ways to avoid the error. The company said federal officials seized about 1,300 pumps from a manufacturing plant in San Diego; about 140,000 such pumps have been distributed worldwide.

Related articles
Parker Waichman Accolades And Reviews Best Lawyers Find Us On Avvo