MiniMed Paradigm Insulin Pumps: Recall & Information

Get Legal Help Today

 Secured with SHA-256 Encryption

Jeffrey Johnson is a legal writer with a focus on personal injury. He has worked on personal injury and sovereign immunity litigation in addition to experience in family, estate, and criminal law. He earned a J.D. from the University of Baltimore and has worked in legal offices and non-profits in Maryland, Texas, and North Carolina. He has also earned an MFA in screenwriting from Chapman Univer...

Full Bio →

Written by

UPDATED: Jul 16, 2021

Advertiser Disclosure

It’s all about you. We want to help you make the right legal decisions.

We strive to help you make confident insurance and legal decisions. Finding trusted and reliable insurance quotes and legal advice should be easy. This doesn’t influence our content. Our opinions are our own.

Editorial Guidelines: We are a free online resource for anyone interested in learning more about legal topics and insurance. Our goal is to be an objective, third-party resource for everything legal and insurance related. We update our site regularly, and all content is reviewed by experts.

Medtronic MiniMed Paradigm Insulin Pumps have undergone two recalls in their history. In 2004, Medtronic recalled over 160,000 MiniMed Paradigm Insulin Pumps due to a defective tube. That episode led to at least 200 diabetic patients being injured and/or hospitalized, and at least one fatality, when a diabetic user of the Paradigm insulin pump lost consciousness while driving and crashed.

The most recent recall of MiniMed Paradigm Insulin Pumps took place in July of 2009. This recall, also due to defective tubes in the device, covered approximately 60,000 tubes that were distributed under reference numbers MMT-396, MMT-397, MMT-398, and MMT-399, and with lot numbers beginning with the number 8.

Suffered harm from a Defective Medtronic Minimed Insulin Pump? You may have a lawsuit. Click here, for a top rated law firm to evaluate your legal rights. [Sponsored link]

The 2009 recall was made voluntarily by Medtronic, but the FDA still issued its own comments on the defective tubes. The FDA categorized the recall as the most serious type possible (Class 1), which involves situations in which there is a reasonable probability that use of the product will cause serious injury or death. The FDA further stated that the reason for the recall was that the tubing, known as “infusion sets,” may not allow the insulin pump to vent air pressure properly, which could potentially result in the device delivering too much or too little insulin, and cause serious injury or death.

It is important to note that Medtronic’s recall asks that consumers return the defective products to Medtronic for a replacement. This is not a problem if the product has not caused anyone any harm. However, if the device has caused harm and there is a potential legal claim involved, the defective device should be kept as evidence. Of course, no one should use the device if it is defective. A new device may be needed. For full text of the MiniMed Paradigm Insulin Pump press release, click here.

If you or a loved one has suffered harm from use of one of Medtronic’s defective insulin tubes, seek legal help immediately to protect your rights. While there is no fee or obligation, delaying may cause you to lose your right to seek compensation for injuries caused by MiniMed Paradigm insulin pumps due to state-imposed time limits for filing a lawsuit.

Check out the following articles for more information about MiniMed Paradigm Insulin Pumps, filing a MiniMed Paradigm Insulin Pump lawsuit, and finding a MiniMed Paradigm Insulin Pump attorney.

Suffered harm from a Defective Medtronic Minimed Insulin Pump? You may have a lawsuit. Click here, for a top rated law firm to evaluate your legal rights. [Sponsored link]

Get Legal Help Today

Find the right lawyer for your legal issue.

 Secured with SHA-256 Encryption