What to Expect in Medical Procedures Involving Total Hip Recall

Most probably, a lot of hip replacement patients have already heard about the announcement made by DePuy Orthopaedics Inc. on its issuance of urine collection bag, specifically involving two of its defective ASR hip replacement products - the DePuy ASR hip resurfacing system and the DePuy ASR XL acetabular system.

With more than 93,000 patients being affected by such defective medical devices (making it one of the high profile medical device recalls in the history of the hip replacement industry) one way or another, such news must have reached every individual involved in the DePuy ASR recall.

Several individuals implanted with the defective product now subject to DePuy ASR recall have reported varying bodily complications that entail debilitating pain, swelling in the hip area and walking discomfort. Moreover, because of the probable presence of laryngeal mask airways
Note that patients implanted by the recalled hip implant products that are now subject to DePuy ASR recall should undergo some procedure to ensure their safety. It is, thus, imperative that concerned individuals must see their doctor as soon as possible so that they could be checked for the stability of the hip replacement device used in their surgical procedure.

The medical examination procedure entails that the patient implanted with the recalled hip replacement who experiences pain, discomfort in walking and other symptoms, will have to undergo radiologic (X rays) examination in order to assess the extent of the damage brought by the device.

There are a number of reasons that may have caused these symptoms, such as the loosening of the device, dislocation and bone fractures. Whenever it is determined that the damage caused by the device is already large, the doctor may recommend that the patient undergo a second surgery, also known as revision surgery. This procedure involves the removal of the defective device and replaced by another device.

Other examinations may involve having the patient's blood tested for the presence of metal debris in the blood. If the amount of metal ion is greater than what the human body can normally take, it is possible that the patient may suffer serious complications such as pseudo tumors and chromium and cobalt poisoning. The seriousness of this condition is enough reason for patients to act immediately since delays could lead to a greater chance of worsening complications. This is why every individual who has undergone a hip replacement procedure must take the DePuy ASR recall seriously.

Individuals who have had their hips replaced before July 2003 - the manufacturing and distribution date of the hip replacement products subject to the DePuy ASR recall - may be affected by the said total hip recall. It is, therefore, necessary that they should see a doctor for proper care and a lawyer for high flow nasal cannula oxygen of compensation from the manufacturer.