OxyTOTE Lawsuit | 2025 Latest Updates

The U.S. Food & Drug Administration (FDA) has announced a Class I Recall for the OxyTOTE portable oxygen system, a medical apparatus intended for assisting patients with their breathing needs during travel. If not handled properly or if accidentally dropped, there is a risk that the oxygen device could catch fire and explode, leading to severe injuries or fatalities.

What’s the Problem?

The OxyTOTE portable oxygen system legal actions involve defective medical devices that can ignite and explode when mishandled or dropped. The primary allegations against Western/Scott Fetzer Company focus on the dangerous fire and explosion risks posed by these pressurized oxygen systems.

Latest OxyTOTE Recall Updates

• January 31, 2015 – The FDA initiated a Class I recall of OxyTOTE Portable Oxygen System regulators and Valve Integrated Pressure Regulators manufactured by Western/Scott Fetzer Company. The recall was due to the risk of ignition and explosion of compressed gas oxygen cylinders, which could cause serious injury or death if the device was dropped or mishandled. A total of 162,678 units manufactured and distributed from January 1, 2009 to September 30, 2014 were affected [1].

FDA Reports and Statistics

The FDA received reports of at least 2 device malfunctions, with a 50% fatality rate among reported incidents.

OxyTOTE Injuries & Hazards

The recalled OxyTOTE portable oxygen systems have been linked to serious injuries and deaths due to fire and explosion risks. Reported injuries and complications include:

• Severe Burns: Flash fires from internal ignition causing extensive burn injuries
• Explosion Injuries: Burst canisters causing traumatic injuries from flying debris
• Fatalities: Deaths resulting from device malfunctions during normal use
• Property Damage: Fire damage to surrounding areas and personal belongings

Do You Qualify for an OxyTOTE Lawsuit?

You may qualify for an OxyTOTE lawsuit if:

• You used an OxyTOTE portable oxygen system between 2009-2014
• You experienced serious injuries including burns, explosion injuries, or death occurred
• The injuries required medical treatment or hospitalization
• You can provide medical documentation linking your injuries to the OxyTOTE device
• You have proof of device ownership or use through medical records

Evidence Required for an OxyTOTE Lawsuit

To build a strong case, you will need:

• Medical records documenting your injuries and treatment
• Documentation proving use of the OxyTOTE device (prescriptions, medical orders, hospital records)
• Proof of device serial numbers or model information
• Witness statements if others were present during the incident
• Photos of the device and any property damage
• Medical expert testimony linking injuries to device malfunction

Damages You Can Recover

Compensation in OxyTOTE lawsuits may include:

• Medical expenses for emergency treatment, surgery, and ongoing care
• Lost wages and reduced earning capacity
• Pain and suffering from burn injuries and trauma
• Punitive damages against the manufacturer for defective design
• Wrongful death damages for surviving family members
• Property damage from fires caused by device malfunction

OxyTOTE Recall Information

The FDA issued a Class I recall on September 30, 2014, affecting 161,674 OxyTOTE portable oxygen system regulators and valve integrated pressure regulators. Recalled models include OxyTOTE, oxyQuik, and AirTOTE products manufactured by Western/Scott Fetzer Company. The recall covers devices distributed from January 1, 2009 to September 30, 2014, primarily used in hospitals, nursing homes, and medical clinics.

The following model numbers are subject to the recall:

• AAG-403

• AAG-800

• AAG-802

• AAG-803

• GTS-303

• GTS-4206

• GTS-600

• GTS-603

• JHR-900

• JHR-LG-MTS-903

• LAW-603

• MNR-3000

• MNR-600

• MNR-800

• MNS-602

• MNS-603

• MNS-803

• MNS-C803

• MTR-100

• MTR-300

• MTR-500

• MTR-600

• MTR-700

• MTR-800

• MTS-303

• MTS-403

• MTS-501

• MTS-502

• MTS-503

• MTS-505

• MTS-601

• MTS-602

• MTS-603

• MTS-803

• OXC-503

• PHS-LG-MTS-803

• ROC-9792

• ROC-9793

• RRI-500

• RRI-600

• TRI-803

• VLB-603

• VLB-603H

• VNG-600

• VNG-603

• VNG-800

• WOX-603

All units of these models produced before October 1, 2014, are included in the recall

Statute of Limitations for OxyTOTE Lawsuits

Time limits for filing OxyTOTE lawsuits vary by state but typically range from 2-4 years from the date of injury or discovery of harm. Given that the recall occurred in 2014, it’s critical to act quickly as statute of limitations deadlines may be approaching. Some states have specific provisions for product liability cases that may extend filing deadlines, but immediate legal consultation is essential to protect your rights.

FAQs

1. How can I join the OxyTOTE portable oxygen system lawsuit?

To join the OxyTOTE portable oxygen system lawsuit, you should contact a law firm specializing in product liability or medical device litigation. They will assess your situation and guide you through the process of filing a claim.

2. What compensation might be available through the OxyTOTE portable oxygen system lawsuit?

Compensation may include medical expenses, lost wages, pain and suffering, and damages related to injuries or deaths caused by incidents involving the OxyTOTE system. Compensation for property damage may also be available.

3. What should I do if a loved one was killed due to an incident involving the OxyTOTE system?

If a loved one was killed in an incident involving the OxyTOTE system, you may have grounds to file a wrongful death lawsuit. Consulting with a lawyer who specializes in such cases is essential to explore your legal options.

4. Which OxyTOTE models are affected by the recall?

The recall affects OxyTOTE, oxyQuik, and AirTOTE portable oxygen systems manufactured between January 1, 2009 and September 30, 2014. Check the FDA recall database for complete lot and model numbers.

5. What caused the OxyTOTE devices to malfunction?

The devices can ignite when mishandled or dropped, causing internal flash fires and canister bursts. The manufacturer received reports of malfunctions including one death and one injury.

6. How long do I have to file an OxyTOTE lawsuit?

Statute of limitations varies by state, typically 2-4 years from injury date. Given the 2014 recall, immediate legal consultation is crucial to protect your rights.

7. What evidence do I need for an OxyTOTE lawsuit?

You’ll need medical records, proof of device use, documentation of injuries, and any available photos or witness statements from the incident.

8. Are there any settlements in OxyTOTE cases?

Settlement information is often confidential, but experienced product liability attorneys can provide insight into potential compensation based on similar medical device cases.

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Get A Free OxyTOTE Lawsuit Evaluation With Our Lawyers

Time is limited to pursue legal action against the manufacturers of defective OxyTOTE portable oxygen systems. With the recall dating back to 2014, statute of limitations deadlines may be approaching rapidly in many states.

The Medical Device Litigation Group at our law firm is an experienced team of trial lawyers that focus on the representation of plaintiffs in OxyTOTE Lawsuits. We are handling individual litigation nationwide and currently accepting new injury and death cases in all 50 states.

Our legal services include:

• Free, confidential consultations to evaluate your case
• No upfront costs or fees – we only get paid if we win your case
• Experienced medical device litigation attorneys
• Nationwide representation for OxyTOTE injury claims

Reference:

https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=132378.