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Sundquist Amadi

Case type 02

Defective medical devices

Implants and devices that failed, broke apart, or had to come out early.

Section 1 · Identification

Claim is against
The device maker, and sometimes its distributor
Key evidence
The implant record from your operative report, and records of any revision surgery
Usual form
Often grouped in an MDL, with some cases in state courts

Section 01: Overview

What a device case is.

Device cases cover hardware placed in or on the body: joint implants, mesh, filters, pumps and stimulators. The claim is against the company that designed or made the device.

Having a device that was later recalled is not a case on its own. What usually matters is a real complication, and most often a revision, removal or repair surgery. We help you find the make and model, which many people have never seen.

A man on crutches with a surgical dressing on his knee, standing in a doorway at home
Fig. 1 Revision surgery is the fact most device cases turn on.

Examples of what we review

  • A metal hip implant that loosened and shed debris (example)
  • A hernia mesh device that shrank or moved (example)
  • A filter placed in a large vein that tilted or broke (example)
  • A knee replacement part that failed early (example)
  • A spinal cord stimulator that shifted or overheated (example)

Generic examples on a demo site. No real product, company or lawsuit is named.

Section 02: What we look for

Most cases that move forward have these.

Missing one is not always the end. Some facts can be found in records you have forgotten about. We will tell you which ones matter for you.

Usually a fit

  • Fit: You had a revision, removal or repair surgery, or a surgeon has recommended one
  • Fit: Your records name the device maker and model (we can help find this)
  • Fit: The failure matches problems in recalls, safety notices or published research
  • Fit: Your problems began after the device was placed

Usually not a fit

  • Not a fit: The device is working and you have no symptoms (worry alone is not a case)
  • Not a fit: The problem came from how the surgery was done rather than the device (that may be malpractice)
  • Not a fit: No record anywhere can identify the device

Section 03: Records that help

What to gather, and how to get it.

You do not need any of this before you call. With your written permission, we can request most of it for you.

  1. 01 Implant card or patient ID card

    Many patients get one at discharge. It is often in the discharge folder or a wallet.

  2. 02 Operative report and implant log

    The hospital's surgery record usually includes a sticker page listing the maker, model and lot number of every part.

  3. 03 Revision surgery records

    The report from the surgery that repaired or removed the device, plus any pathology report on what was removed.

  4. 04 The removed device itself

    Ask the hospital in writing, before or right after surgery, to keep the device and not send it back to the maker.

Section 04: Your filing window

The clock may start when you found the problem.

Section 05: How these cases run

What to expect, honestly.

Device cases with many similar claims are often grouped in an MDL for evidence gathering and early trials. Your case keeps its own facts and medical history. Device cases tend to take years, and we tell you that at the start.

How group cases work

Section 06: Finding your implant

Where the model number hides.

Most people have never seen the make or model of their implant. It is almost always written down somewhere. These are the four places we look first.

Parts of a hip replacement A cup set into the pelvis holds a liner. A ball sits in the liner and joins a neck and stem that run down inside the thigh bone. 1 2 3 4 CUP (SHELL) LINER BALL (HEAD) STEM Set into the pelvis Plastic, ceramic or metal Metal or ceramic Inside the thigh bone
  1. 1Cup (shell), set into the pelvis
  2. 2Liner, plastic, ceramic or metal
  3. 3Ball (head), metal or ceramic
  4. 4Stem, inside the thigh bone
Fig. 3 Illustration, not to scale. A hip replacement usually has four parts, and each can come from a different model line. The implant log from your surgery lists every one.
  1. 1 Implant card A wallet card or sticker sheet some patients get at discharge.
  2. 2 Implant log A page in the operative report with peel-off stickers for every part, showing maker, model and lot.
  3. 3 Hospital bill Itemized bills often list each implanted part as its own line.
  4. 4 Surgeon's office The office keeps the operative report and can send it with your written OK.

Section 07: Questions

Questions about device cases.

Is this a class action?

Usually not. Most device cases are individual cases grouped for pretrial work in an MDL. In a class action, one case speaks for everyone. In an MDL, each person keeps their own case and their own outcome.

My surgeon says the device was fine. Should I still call?

You can. Surgeons judge your health, not a legal claim. If the device was removed or repaired, the records will show why, and we can read them with you.

The hospital kept my removed device. Can I get it?

Often, yes. We send a written request asking the hospital to hold it and not return it to the maker. The sooner the request goes out, the better.

All questions

Free case review

Talk to someone who reads the file.

A free review takes about ten minutes. You get a plain answer: yes, not yet, or no, with the reason. Contacting us does not make you a client and costs nothing.

Start a free case review Call (612) 555-0148

Mon to Fri 8 to 6 · Sat 9 to 1 · No fee unless money is recovered

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