Synthes Recalls Bone Putty Over Ignition Concerns

Orthopedic device manufacturer Synthes has issued a voluntary Class I recall of its Hemostatic Bone Putty, according to an FDA news release.

Advertisement

 

Sign up for our FREE E-Weekly for more coverage like this sent to your inbox!

Hemostatic Bone Putty is designed to stop bone bleeding by establishing a physical barrier along the edges of bones that have been damaged by trauma or cut during a surgical procedure.

Synthes has recalled all lots of the bone putty, citing potential for the product to ignite when in contact with electrosurgical cautery systems. The Class I category is the most serious type of recall since it can cause serious adverse events or death.

More Articles on Patient Safety:

Covidien Recalls Electrode Kits

ATP Values Help Determine Endoscope Cleanliness

Number of Central Lines Could Alter Infection Rates

At the Becker's 23rd Annual Spine, Orthopedic and Pain Management-Driven ASC + The Future of Spine Conference, taking place June 18–20 in Chicago, spine surgeons, orthopedic leaders and ASC executives will come together to explore minimally invasive techniques, ASC growth strategies and innovations shaping the future of outpatient spine care. Apply for complimentary registration now.

Advertisement

Next Up in Uncategorized

Advertisement

Comments are closed.