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Do Not Use Ultraviolet (UV) Wands That Give Off Unsafe Levels of Radiation

Sep 1, 2022 | Product Liability, Uncategorized

The U.S. Food and Drug Administration (FDA) continues to warn consumers about the potential risk of injury associated with the use of certain brands of ultraviolet (UV) wands. Do not use these UV wands because they may expose you or any nearby person to unsafe levels...

CereLink ICP Monitor by Integra: Class I Recall – Due to Risk of Incorrect Intracranial Pressure Readings

Aug 31, 2022 | Medical Malpractice, Product Liability, Uncategorized

Integra is recalling the CereLink ICP Monitor, Model #826820/826820P, after reports that the device may display incorrect values for a patient’s intracranial pressure and display out-of-range pressure readings. If the device is not working properly, the patient may...

Medtronic Recalls HeartWare HVAD System Batteries for Electrical Faults That Cause Battery Failure

Aug 25, 2022 | Medical Device Failure, Medical Malpractice, Product Liability, Uncategorized

Medtronic, Inc. is recalling HeartWare HVAD System batteries because the batteries may experience electrical faults that cause them to unexpectedly fail. When this occurs, batteries with an electrical fault may be unable to power the controller, unable to accept...
Homeopathic Teething Tablets

Homeopathic Teething Tablets

Jan 30, 2017 | Medical Malpractice, Product Liability, Uncategorized

FDA issues new warning against homeopathic teething tablets The U.S. Food and Drug Administration (FDA) is warning against the use of homeopathic teething tablets after lab analysis found inconsistent amounts of belladonna, a toxic substance that could post a risk to...
Medtronic Announces Recall Of Several Neurovascular Products Due To Blood Clot Risk

Medtronic Announces Recall Of Several Neurovascular Products Due To Blood Clot Risk

Oct 17, 2016 | Medical Device Failure, Product Liability, Uncategorized

The Wall Street Journal reported that Medtronic has announced a recall of specified lots of four neurovascular products because they can cause an increased risk of blood clots. Specifically, the recall includes the company’s Pipeline embolization device, Alligator...
Button Battery from Vizio Remote Causes Severe Injury to Toddler

Button Battery from Vizio Remote Causes Severe Injury to Toddler

Feb 28, 2014 | Plaintiff’s Law, Product Liability, Uncategorized

Last year a one year old in Austin, Texas accessed a coin shaped “button” battery from a Vizio stereo bar remote control and ingested it. The battery lodged in his esophagus and the electric current created a caustic agent that burned his throat tissue. This serious...
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  • Microdosing Chocolate Bars by Diamond Shruumz-Brand: Investigation of Illnesses – Do not eat, sell, or serve Diamond Shruumz- Brand Microdosing Chocolate Bars. FDA’s investigation is ongoing.
  • Abbott Recalls Amplatzer Steerable Delivery Sheath for Increased Risk of Air Embolism #3
  • Abbott Recalls Amplatzer Steerable Delivery Sheath for Increased Risk of Air Embolism
  • The Danger of Infant Head Shaping Pillows
  • Do Not Use Ultraviolet (UV) Wands That Give Off Unsafe Levels of Radiation


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