Reich & Binstock
Free Initial Consultation Call
713-352-7883
713-352-7883

How can you tell how serious a medical device recall is?

Medical device recalls can happen for a variety of reasons. Although some manufacturers voluntarily recall their products, the U.S. Food and Drug Administration (FDA) often has to issue an order to remove the item from circulation or use.

A voluntary recall occurs when the manufacturer removes the product from the marketplace to correct an alleged violation of FDA regulations. A mandatory device recall is when the federal agency issues a recall order because they believe that it's putting the health of the public at risk. Although this type of event seldom occurs, the FDA does this in instances where the manufacturer fails to voluntarily recall the product themselves.

There are three types of recall classifications. A Class I recall is when there's a reasonable probability that a device will cause serious harm or even death. The FDA may order a Class II recall if they believe that a product may cause temporary or reversible adverse medical consequences. The least critical recall is a Class III. It's unlikely to cause poor health outcomes.

The public can find out about any recalls in the federal agency's weekly FDA Enforcement Report. It's there that they inform readers about any field corrections, injunctions, recalls or seizures. The federal agency often rescinds recalls if they see that the manufacturer has made reasonable efforts to remove the device from circulation themselves or that any potential flaws are corrected.

A recall strategy factors in different plans of actions and approaches based upon the individual circumstances surrounding each device. Some considerations will include the results of the health hazard evaluation. Others will take into account how easy it is to identify the product or how obvious it is to the average consumer or user that it has a deficiency. Regulators also often consider how likely it is that consumers will use the device.

If you have sustained severe adverse health consequences after being outfitted with a now-recalled medical device, you may be entitled to monetary compensation for your medical bills and the decline in your quality of life. The amount of financial reimbursement that you may qualify to receive will likely vary depending on the extent of your losses. A defective medical device attorney can evaluate your case and recommend the best way to proceed with it.

No Comments

Leave a comment
Comment Information
Email Us For A Response

Contact Us For a Free Legal Consultation There is a never a fee unless we recover on your behalf.

Bold labels are required.

Contact Information
disclaimer.

The use of the Internet or this form for communication with the firm or any individual member of the firm does not establish an attorney-client relationship. Confidential or time-sensitive information should not be sent through this form.

close

Privacy Policy

Call for a Free Legal Consultation: 713-352-7883
Reich & Binstock - Pharmaceutical Injury & Class Action Lawyers

4265 San Felipe
Suite 1000
Houston, TX 77027

Toll Free: 877-643-3099
Phone: 713-352-7883
Fax: 713-623-8724
Houston Law Office Map