DePuy Orthopaedics Regulatory Problems with Hips, Knees Draw FDA Warning
Federal regulators are accusing Depuy Orthopaedics, a subsidiary of Johnson & Johnson, of selling artificial knee and hip replacement implants without approval.
The FDA issued a warning letter to DePuy Orthopaedics last month about the regulatory problems, after inspectors visiting a plant in Warsaw, Indiana discovered a host of implants being manufactured there that were never given FDA approval.
The letter, released this week by the FDA, has forced DePuy to remove 14 different implant components from the market until the issue can be resolved.
Did You Know?
Millions of Philips CPAP Machines Recalled
Philips DreamStation, CPAP and BiPAP machines sold in recent years may pose a risk of cancer, lung damage and other injuries.Learn More
DePuy officials told FDA investigators that the components found at the plant were custom devices made for specific patients’ anatomies, and thus did not have to get premarket approval, even through the agency’s fast-track 501(k) approval process. However, the agency disagrees, saying that none of the devices qualify as custom devices.
“Although the devices’ size and shape may vary with each patient’s anatomy, the standardized design characteristics do not vary among the devices manufactured,” the FDA concluded. “The fact that final specifications are tailored to match a patient’s anatomy does not preclude a clinical study or submission of a marketing application for the devices.”
Not only should the devices not have been sold, but they were manufactured with poor quality control procedures, the FDA warning letter notes. The letter cites the company for using poor design validation procedures, not having a process in place for handling customer complaints and other regulatory violations.
DePuy Orthopaedics was the focus of a major artificial hip system recall in August 2010 when it pulled 93,000 ASR metal hip implants from the market. The ASR hip recall has triggered more than 3,500 lawsuits against the company.
At the time of the recall, Johnson & Johnson indicated that the DePuy ASR failure rate was about 12%. However, some expects have suggested that the actual percentage of people who are likely to experience problems with their implant, including loosening, metal poisoning and possible revision surgery, is going to be substantially higher as more time passes.
Since the recall, a growing flood of DePuy ASR hip implant lawsuits have been filed against Johnson & Johnson in state and federal courts throughout the United States. The federal DePuy ASR litigation has been consolidated for pretrial proceedings in the U.S. District Court for the Northern District of Ohio as part of an MDL, or multidistrict litigation.
JosephOctober 18, 2016 at 8:02 pm
I had 3-total knee replacements in a 8- year span.. Because of faulty Depuy equipment..
"*" indicates required fields
More Top Stories
A federal judge has approved a plan appointing several dozen plaintiffs' attorneys to leadership positions in Bard Port Catheter litigation.
A ProPublica report reveals that Philips officials hid thousands of reports of problems with sound abatement foam used in millions of CPAP machines, failing to recall the devices for more than a decade after receiving the first complaints.
A Suboxone lawsuit claims the opioid addiction treatment's dental side effects can lead to severe tooth damage and decay.