As part of a facility's sharps injury prevention program, it is valuable to help product evaluation teams or committees determine how devices are used in their healthcare organization.
The Latest
The total market for advanced orthopedic technology and products was estimated to exceed $28 billion in 2010, according to a MarketResearch news release.
The American Academy of Ambulatory Care Nursing has released a position statement advocating for registered nurses' roles in ambulatory care.
Triad lubricating jelly products, distributed by Triad from Jan. 2007-Dec. 2010, have been recalled due to potential sterilization problems, according to an FDA news release.
Robotic-assisted partial knee replacement may be a viable choice for patients with osteoarthritis of the knee, according to an MD News report.
Although wearing surgical scrubs outside a healthcare facility is generally acceptable, leaders in infection control and prevention are trying to flip the switch on the potentially dangerous practice, according to a Pittsburgh Tribune-Review news report.
ArthroCare, a maker of minimally invasive surgical products, has received FDA clearance for its second-generation Parallax Contour-enhanced vertebral augmentation device, according to a news release.
Johnson & Johnson has recalled lots of its Simponi injections for possible substandard dosage of its arthritis treatment, according to a Reuters news report.
Florida State Representative Patrick Rooney, (R-Palm Beach Gardens), has proposed legislation that would bar pharmacies from being within a 10-mile radius of pain clinics, according to a Palm Beach Post news report.
House legislators heard arguments over the FDA's regulatory process, with opposing arguments stating the approval process of medical devices is either too slow or too quick, according to a Washington Post news report.
