Medtronic Synchromed II Recall

We Are Taking Cases For Defective Medtronic Synchromed II Infusion Pumps
 
 
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Medtronic Synchromed II Recall
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Medtronic SynchroMed II Recall | Call Us To Discuss Your Case

Have you suffered a serious injury or lost a loved one due to a defective Medtronic Synchromed II Infusion Pump?

Suffering from chronic pain can be a major daily challenge for people across the country. Medical devices, like infusion pumps, aim to help people with pain relief. Unfortunately, when medical devices of this nature are defective, the impacts can be detrimental. In 2019, the infusion pump Medtronic SynchroMed II was recalled for causing serious harm to users.

If your health has been negatively impacted by a Medtronic SynchroMed II, you need a trusted legal team to help you recover the compensation and justice you deserve. With over 50 years of combined legal experience, the attorneys at Brock & Goetzmann can help you recover the compensation you are entitled to after suffering from burdens caused by a defective infusion pump. For a skilled legal team committed to helping you find justice after being hurt by a Medtronic SynchroMed II, call Brock & Goetzmann today.

The Medtronic SynchroMed II, a popular drug infusion pump, was recalled by the U.S. Food & Drug Administration in 2019. These pumps were distributed to patients between May 11, 2018, and September 5, 2019. There were over 7,300 devices covered under this recall. The pump was recalled because of a permanent motor stall, which could prevent drugs to be properly infused. The motor stall issue occurred as a result of foreign particles that were inside of the pump motor assembly. If you have had a Medtronic SynchroMed II installed during the dates listed above, it is important that you consult with your healthcare provider as soon as possible. Don’t wait, call the Medtronic Synchromed II recall attorneys at Brock & Goetzmann today!

 

Issues Caused by Defective Infusion Pumps

There are several other issues commonly associated with defective infusion pumps. The first issue is battery failure due to film buildup, which can make it so patients are not getting the amount of medicine they need. Another issue with defective infusion pumps is that pocket fills may occur. When pocket fills happen, the dosage is injected into the skin instead of into the device, which can result in an unintentional and possibly fatal overdose. When an incorrect dosage of medicine is administered, either over or under the needed amount, a patient can suffer from very difficult symptoms. These may include the following:

  • Seizures
  • Itching
  • Low blood pressure
  • Tingling sensations
  • Loss of consciousness
  • Return of pain or previous symptoms

Know Your Legal Rights!

If you were issued a faulty Medtronic Synchromed II, you need an attorney who is ready to fight for you. With over 50 years of combined experience, the legal team at Brock & Goetzmann can help you get started on a claim against Medtronic. All you have to do is give us a call. When it comes to pursuing justice, don’t hesitate to contact Brock & Goetzmann. We are ready to help when you need us most!

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