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Birth Injury
Is it Malpractice When a Material Infection Causes Cerebral Palsy?
How Cerebral Palsy Affects Development of Children in Kentucky & Ohio
Kentucky Birth Injuries Caused by Obstetric Forceps
Pitocin and Kentucky Birth Injuries
Kentucky Birth Injuries Caused by Vacuum Extractions
Semi-Truck and Auto Accidents
Kentucky Car Accidents and Drowsy Driving
Cell Phones and Kentucky Car Accidents
Defective Maintenance Issues Can Cause Kentucky Truck Wrecks
Texting Ban on Kentucky Motorists passed by House
Dangerous and Defective Products
Drugs for Osteoporosis Prescribed Unecessarily?
Defective Children’s Products & Toys are Constantly Recalled
Food manufacturers make consumers responsible
Defibrillator recalled by ZOLL Medical Corporation
Medical Mistakes
Fewer complications from heart device specialists
Pain Pumps
Daubert Motion in Pain Pump Case Found for Plaintiff
Shoulder Pain Pump Manufacturer I-Flow Settles Lawsuits
Shoulder Pain Pump Manufacturers Have Been Silent
Pain Pumps: FDA Requires Warning that Use in Joint Causes Chondrolysis and Cartilage Damage
General
Yaz and Yasmin May Cause Stroke
Taking Yaz or Yasmin May Cause Deep Vein Thrombosis
Yaz Can Lead to Irregular Heartbeat
Hyperkalemia is a Potential Complication of Yaz Birth Control
Lawsuit Filed Against Bayer for Misrepresenting Safety and Effectiveness of Yaz
News
Roman Shades Sold by Pottery Barn Kids Recalled...
Advisory panel recommends ban on pain relievers...
Doctor investigated for Medtronic consultation...
FDA recalls Biosite Triage Cardiac Panel...
FDA warns of contaminated products...
FDA recalls contaminated pistachios...
FDA says stop using Hydroxycut now...
FDA discusses medical device controversies...
Library
Birth Injury
Cerebral Palsy can be Caused by a Maternal Infection
When Newborn Jaundice Becomes Serious – What Every Kentucky Parent Should Know
Cerebral Palsy’s Impact on the Development of Children in Kentucky & Ohio
Nothing is More Heart Wrenching Than Seeing The Consequences of a Prolapsed Umbilical Cord
Did You Know That Pitocin Can Cause Serious Birth Injuries?
Semi-Truck and Auto Accidents
Tired Truckers are a Danger to People on Kentucky Highways
Avoid a Kentucky Car Accident Caused by Drowsiness
Don't Ignore a Head Injury Following a Kentucky Auto Accident
Ten Factors That Can Lead to a Serious Kentucky Truck Accident
Cell Phones Are Blamed For Many Kentucky Car Accidents
Dangerous and Defective Products
Kentucky Lawsuits Filed Over Toyota’s Defective Accelerator Pedal
Fosamax osteoporosis drug prescribed when women only has osteopenia
Zicam cases in Kentucky and Ohio
Fentanyl pain patch being abused
Medical Mistakes
Common Drug Errors to Watch Out For
One in Fifteen Children Injured by Medicine Mistakes
One in 50 Heart Attack Victims Sent Home by Emergency Room Doctors
Surgical Errors Cost Billions of Dollars Every Year
How to prevent medical mistakes
Pain Pumps
PAGCL & Shoulder Pain Pumps: What a Recent Study Reveals
Recent News Regarding Pain Pump Cases
Pain Pumps Used After Knee Surgery Can Cause Damage
Know the Symptoms of PAGCL, Especially if You Used a Shoulder Pain Pump
Medical Studies Find a Link Between Pain Pumps and Chondrolysis
General
Signs and Treatment of Kidney Failure
Yaz or Yasmin Birth Control Can Cause Deep Vein Thrombosis
Symptoms of Pulmonary Embolism Caused by Yaz and Yasmin Birth Control
Defibrillator recalled by ZOLL Medical Corporation
Attorney Ronald E. Johnson of Schachter & Hendy concentrates on legal issues regarding defective medical devices. According to the Consumer Product Safety Commission, the ZOLL AED Plus Defibrillator was recently recalled because it was defective. The medical device was manufactured by ZOLL Medical Corporation from May 2004 through February 2009 and distributed from May 2004 through February 9, 2009. It is possible that between 80,000 to 180,000 units are affected.The ZOLL AED Plus Defibrillator is used by emergency or medical personnel and others who have completed CPR AED training courses. The medical device is intended to treat patients who are undergoing cardiac arrest. It analyzes an unconscious person's heart rhythm and delivers an electrical shock to the heart to restore a normal heart rhythm.
This device is affected by a Class 1 recall -- the most serious type of recall and involves situations in which there is a reasonable probability that use of these products will cause serious injury or death. The defibrillator was recalled because the AED failed to deliver the defibrillation energy. Some batteries do not work properly when used with the ZOLL AED Plus Defibrillator below the units below the serial number X_ _ _200000. The serial numbers above X___20000 are not affected by this corrective action as they contain the updated software that can detect this battery condition and identify when batteries require replacement.
The ZOLL Medical Corporation informed rescue workers that in the event that the AED Plus fails to work, they should immediately resume CPR, and retry the ADI Plus after switching it off and then on again after 10 seconds so the device can reset.
According to a letter sent to consumers by ZOLL, they recommend an update of the device software. The new software can be ordered or downloaded at no cost at http://www.ZOLLAEDPlusbatteryhelp.com. The website also provides other technical information and support concerning this corrective action, such as ordering of replacement batteries. Consumers should use a Personal Computer running Windows XP or Windows 2000 that is equipped with an IrDA (infrared) port. Load the ZOLL Administrative Software (ZAS) onto your PC from either the ZOLL download site, or by ordering a CD from ZOLL. To do either, visit http://www.ZOLLAEDPlusbatteryhelp.com.
Consumers can contact the ZOLL Medical Corporation at:
269 Mill Road
Chelmsford, Massachusetts 01824
http://www.ZOLLAEDPlusbatteryhelp.com
1-978-421-9655
Health care professionals and consumers may report adverse reactions or quality problems experienced with the use of these products to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by FAX.
* Online: http://www.fda.gov/MedWatch/report.htm
* Regular Mail: use postage-paid FDA form 3500 available at: http://www.fda.gov/MedWatch/getforms.htm
Mail to MedWatch 5600 Fishers Lane, Rockville, MD 20852-9787
* FAX: 1-800-FDA-0178
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Schachter, Hendy & Johnson, Attorneys At Law
909 Wrights Summit Parkway
Suite 210
Fort Wright, KY 41011
Phone: (859) 578-4444
Fax: (859) 578-4440
Toll Free: (888) 606-5297
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Contact Us
Schachter, Hendy & Johnson, Attorneys At Law
909 Wrights Summit Parkway
Suite 210
Fort Wright, KY 41011
Phone: (859) 578-4444
Fax: (859) 578-4440
Toll Free: (888) 606-5297
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FAQs
Pain Pumps
- Can pain pumps injure knees as well as shoulders?
- How do I know if my shoulder pain is the result of a defective pain pump?