MedStream Infusion Pump Recall Lawyers

The MedStream Infusion Pump recall lawyers at the firm of Kelley Bernheim Dolinsky, LLC have earned an impressive national reputation for their tireless defense of the rights of those victimized by potentially dangerous or defective medical devices. In light of the recent recall of the MedStream Infusion Pump, patients and families who have suffered serious injury or even wrongful death of a loved one may be able to collect financial compensation for medical expenses, pain and suffering, and additional possible damages resulting from use of this device.

If you or someone you love has been injured or killed as a result of a recalled MedStream Infusion Pump, you could be entitled to substantial financial compensation for your damages. To learn more about your rights, we invite you to contact us at 1-888-554-2889 to speak with an experienced MedStream Infusion Pump lawyer. We offer each of our clients:

  • Free legal consultation with a respected MedStream Infusion Pump recall lawyer
  • Home and hospital visits
  • Flexible scheduling
  • Absolutely no legal fees unless your medical device lawsuit is successful

Problems with the MedStream Infusion Pump

The MedStream Infusion Pump, made by Codman & Shurtleff, is a small medical device which is implanted into a patient’s body so that it can deliver regular doses of Morphine or Baclofen to treat pain, muscle spasms, and stiffness. Unfortunately, it has been discovered that the presence of air in the pump reservoir may cause a higher-than-expected dose of medication into the patient’s system, which can lead to serious and potentially life-threatening consequences, including:

  • Drug overdose
  • Hypotension (low blood pressure)
  • Bradycardia (slow heart rate)
  • Heart arrhythmia
  • Loss of consciousness
  • Death

MedStream Infusion Pump Recall

A Class I recall was issued by Codman & Shurtleff for the MedStream Infusion Pump on October 23, 2013. A Class I recall is the most serious level of recall issued by the FDA, and is only used when it is determined that “there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or death.”

The recalled MedStream Infusion Pumps and Refill kits were all made between March 2009 and September 2012, and distributed from January 2010 to July 2013. Included in the recall are the following products:

  • MedStream Programmable Pump; 20 mL (US: 91-4200)
  • MedStream Programmable Pump; 40 mL (US: 91-4201)
  • MedStream Refill Kit (US: 91-4287)
  • MedStream Refill Kit; 6-Pack (US: 91-4288)

Contact our MedStream Infusion Pump Recall Lawyers

The highly regarded MedStream Infusion Pump recall lawyers at our firm are currently interviewing potential clients for dangerous medical device lawsuits in all 50 states. If you or your loved one has suffered injury or even death resulting from use of this device, please contact us to schedule a free, confidential, and informative consultation with an experienced MedStream Infusion Pump recall lawyer.