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LIFEPAK Defibrillator Recall Lawsuit 

FDA Recall of LIFEPAK Defibrillators

Model: Physio-Control Inc., LIFEPAK 15 Monitor/Defibrillator

Recall Class: Class I

Date Recall Initiated: March 4, 2010

Product(s): LIFEPAK 15 Monitor/Defibrillator

See under Useful Links to search for affected devices by serial number.
The serial number is located on the underside of the device.

These devices were manufactured between March 26, 2009 and December 15, 2009 and distributed between March 27, 2009 and December 15, 2009.

Use: The LIFEPAK 15 monitor/defibrillator is designed for use by trained medical personnel in out-of-doors and indoor emergency care settings to monitor patient heart rhythms and to treat patients experiencing cardiac arrest.

Recalling Firm:
Physio-Control, Inc.
11811 Willows Road NE
Redmond, Washington 98052-2003

Reason for Recall: There is a potential for the device to unexpectedly:

  • Power Off then On by itself.
  • Power Off then NOT turn On.
  • Power Off by itself requiring the operator to turn it back On.
  • Stay powered On and not allow itself to be turned Off.

Public Contact: Physio-Control Technical Support at

1-800-442-1142 - option 5, Monday - Friday between 6:00 A.M. and 4:00 P.M. (Pacific Time).

More information available at http://www.physio-control-notices.com/LP15pcb

FDA District: Seattle

FDA Comments: On March 4, 2010, the company informed customers by letter advising them to keep the device in service and to test their devices according to the operating instructions. The company stated that local service representatives are scheduling service visits within 60 days. Customers were asked to forward the Physio-Control notice to all their responsible parties.

Class 1 recalls are the most serious type of recall and involve situations in which there is a reasonable probability that use of these products will cause serious adverse health consequences or death.

Health care professionals and consumers may report adverse reactions or quality problems they experienced using these products to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by FAX.

LIFEPAK Defibrillator Injury / Death Lawsuit

 

If you or a loved one have been injured or a loved one loved has died as a result of a defective LIFEPAK 15 Defibrillator, then call us to discuss your legal rights to a possible LIKEPAK Lawsuit It is very important that you speak to a lawyer concerning this and what can be done to protect your rights.

 

Call and speak with a Board Certified Personal Injury Trial Lawyer with more that 25+ years of experience and representing seriously injured clients across the United States. Call for a Free & Confidential Case Consultation at 1-800-883-9858 or fill out the Online Form below.

 

Free LIFEPAK Defibrillator Case Evaluation - Talk to a Lawyer / Attorney
Please fill out the form below and we will call or write you back within 12-24 hours or call us at 1-800-883-9858.

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Did a Lifepak Defibrillator cause injury or death?
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Willis Law Firm - Houston, Texas Drug Recall Injury Lawyers Attorneys Free Lawsuit & Class Action Litigation Consultation

 

LEGAL ADVERTISING

THIS WEBSITE IS NOT A MEDICAL SITE

This is an Attorney / Lawyer Advertising Website. It is not a medical information, medical dictionary, medical advice or medical help site. Talk to you own treating Doctor about any questions or concerns that you have concerning any medicine, drug, medical device or treatment plan. Do not rely on any information on this site to alter, stop or change any medication or treatment plan by your prescribing or treating Doctor. Many of the drugs and devices listed here on this site have published risk and warnings associated with their use and have not been recalled. This website is not in anyway connected with any drug company or the FDA.Check with your Doctor, Pharmacy and/or the FDA as to any concerns as to their use, recall status and safety. See http://www.fda.gov/ for the latest information.

 

 

 

 

 

 

 

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Actos has been reported to increased the risk of bladder cancer with extended usage see Actos Bladder Cancer , Actos Bladder Cancer Lawsuit . Many women are suffering from serious complications from transvaginal mesh complications, bladder sling erosion and ObTape bladder sling erosion. For more information see Mesh erosion and if you took Zoloft while pregnant and you baby was born with birth defects then talk to a lawyer at:  Zoloft Birth Defect Lawsuit and if you took Depakote while pregnant and you child was bron with spina bifida or other neural tube defects then visit Depakote Spina Bifida Lawsuit