Medical Device Litigation

Medical Device
Recalls

Patients trust medical equipment to aid their recovery, not cause further harm. When manufacturers release unsterilized or defective devices, we provide the aggressive advocacy needed to secure justice.

Attorney Osbelia Castillo - Expert in Medical Device & Product Liability Law

Advocating for Victims of Sterile Processing Failures

The Jackson-Pratt (JP) 3-Spring Reservoir is a critical tool used to drain wounds post-surgery. However, recent recalls have highlighted a dangerous lapse in sterilization protocols, placing thousands of patients at risk of life-threatening infections. When a medical device fails to meet basic safety standards, the manufacturer must be held accountable.

In Santa Barbara, we represent individuals who have suffered complications due to these recalled kits. Our firm investigates the timeline of the defect and the manufacturer's failure to warn the public, ensuring that injured patients receive the compensation necessary for additional medical care and recovery.

Recognizing the Risks of JP Reservoir Kits

Post-Operative Infections

Unsterilized equipment can lead to severe surgical site infections, characterized by high fever, redness, and discolored discharge.

Sepsis & Systemic Risks

If a wound infection is not treated aggressively, it can progress to sepsis, a life-threatening condition that leads to organ failure.

Extended Hospitalization

Victims of defective medical devices often face additional surgeries and long-term antibiotic treatments to combat preventable infections.

"Medical safety is a right, not a privilege. We stand with patients to ensure that corporate negligence never goes unchecked."

Osbelia Castillo

With over 50 years of collective legal experience, our team has the resources to take on major medical manufacturers. We operate on a contingency basis, ensuring you have access to premier legal representation without any upfront costs.

Medical Device Recalls: Frequently Asked Questions

Your surgical records and hospital discharge papers will list the specific medical instruments used. We can assist you in obtaining these records to confirm if your device was part of a recalled lot.

Patients should monitor for high fevers, chills, excessive swelling at the wound site, or any unusual discharge. If you experience these symptoms, seek medical attention immediately.

Yes. A voluntary recall does not absolve a company of liability for the harm their product caused before or during the recall process.

You may seek recovery for additional medical bills, lost wages during your extended recovery, pain and suffering, and the long-term impact on your health.

The Defense Advantage

Insurance Expertise

We anticipate insurance company tactics to prevent common claim denial strategies.

Maximum Recovery

Meticulous case preparation designed to secure the highest possible settlements.

Case Submission

Medical Device Recalls