Skip to main content

G5 Ventilator by Hamilton News

Ventilators allow people to breathe if they are unable to breathe on their own due to a medical condition that renders them unable to get enough oxygen to their lungs. A ventilator may be in use for a short period of time after an accident when a patient is temporarily injured. Patients may also need to use a ventilator for a much longer period of time should they have ongoing, chronic medical problems.  Should the ventilator fail to work for more than a few seconds, the patient may suffer possibly serious side effects that may compromise their long-term health.

Ventilator Recall

Ventilator manufacturer Hamilton has issued a recall of the G5 Ventilator V2.00 and V2.31. The FDA considers this the most serious class of recall, indicating that immediate action may be necessary to correct a potentially serious problem of some kind. Officials at the company have issued the recall of the ventilator because it may suddenly stop working without a warning.

Standard Ventilator Alarms

Ventilators work by providing patients with mechanical breathing assistance.  If there is a problem with the ventilator at any point in time, the device is supposed to immediately sound an alarm to let the patient's caregiver know about the problem. This allows the patient to get help breathing while the ventilator is fixed. A caregiver will often be able to help make sure any backup system is working during this time.

The Specific Problem With The G5 Ventilator 

The G5 Ventilator by Hamilton has been recalled because of a report made about a problem with the function of the ventilator.  Ordinarily, the ventilator would immediately sound an alarm when the person who is is supervising the operation of the item presses the device's oxygen enrichment key. The key will be used to help attach the patient's ventilator mask and make sure that it is working correctly. Any problem with the ventilator may occur under certain conditions. Such conditions include when the operator is planning to press the oxygen enrichment key for the second time within 50 milliseconds after any kind of disconnection is found by the caregiver or operator.

Other Times When it May Happen 

This may also happen when any kind of disconnection is detected immediately by the patient's caregiver  but before the important oxygen enrichment period will automatically end on the machine. The result  is that can be there is a problem when the detection of the disconnection issue that is not noticed by the patient's caregiver. There can also be a problem as well as the termination of any oxygen enrichment being used by the patient occur within only 50 milliseconds of each event.  If that is the case and the person who is operating the patient's device does not notice and intervene directly as soon as possible, the patient they have been entrusted to care for may not be able to receive enough oxygen in their lungs. The result can be that the patient may unfortunately suffer from serious adverse health consequences as a result of this malfunction. Those who are working with patients who are using such devices are urged to take steps to help avoid this problem and protect the patients under their care from suffering any adverse effects.

If a Loved One Has Suffered an Injury


The ventilator's malfunction may have caused serious problems to someone you love.  If this is the case for your loved one, it is best it consider consulting with a lawyer about this matter directly as soon as possible.. A lawyer can help anyone who has seen someone they love harmed by the ventilator get access to legal redress. Filing a lawsuit may be necessary to help the injured party get appropriate financial compensation for their pain and suffering.

Popular posts from this blog

News About Phenobarbital Tablets by C.O.Truxton

Do you own a bottle of Phenobarbital Tablets by C.O. Truxton, Inc.?   Maybe you, or someone you know, has been prescribed phenobarbital tablets for sleep, or to control convulsions or seizures. C.O. Truxton, Inc., has recalled Phenobarbital Tablets, 15mg, because someone who bought a bottle of this medication discovered the label had been placed in error on a bottle of this medication with a different dosage strength. The bottle labeled 15mg tablets was actually 30mg tablets. This mistake on the label could potentially cause someone to accidentally take an overdose of phenobarbital. If you take an overdose of phenobarbital, it can cause: your heart to beat too fast  your breathing to be too rapid   you to become pale, weak, and sweat heavily   you to become unconscious   your kidneys to fail, leading to reduced urine, swelling of legs and feet, possibly confusion, shortness of breath  you to fall into a coma  you to need life-saving emergency treatment  Even though onl

Infant Sleep Positioners News

Parents and caregivers are advised to provide adequate comfort during sleep to babies. Sleep is essential for growth and development of a baby. Before birth, an infant spends a tremendous amount of time sleeping. That explains why after birth, babies sleep for long hours. Newborns sleep for approximately 18 hours a day waking up during a diaper change and to feed. In attempting to provide babies comfort when sleeping, some parents use infant sleep positioners. Most parents are unaware of sleeping positioners’ safety and adverse side effects. In this article, we provide an in-depth look at the safety and side effects of infant sleep positioners, anti-roll pillows and nests. Are Sleep Positioners Safe? Sleep positioners, also known as anti-roll or nests do more harm than good. They make babies struggle to breath leading to death. Suffocation is among the leading cause of infant deaths in the United States, accounting for approximately 4,000 mortalities annually according to the Nati

Alka-Seltzer Plus News

In a recent press release by the Food and Drug Administration, Bayer recalled the Alka-Seltzer product out of fear that the ingredients listed on the package might not match the ingredients of the actual product. However, Bayer didn’t voluntarily list the recalled product on its official website and social media account. Therefore, the big question that you should be asking yourself is whether Alka-Seltzer product is safe for your health. FDA noted that the ingredients that were listed on the front of the packaging carton might be different from the ingredients listed at the back of the packaging carton. Although no injuries were reported, the manufacturer was concerned that the labeling errors might lead to a scenario whereby people take substances that they are allergic to causing harm to their health. Most people use Alka-Seltzer products as an over-the-counter drug that temporarily alleviates common symptoms that are associated with cold and flu such as a cough, fever, congestion