Zimmer Biomet SpF Bone Stimulator Recall Issued Due to Cleanliness Concerns
Some Zimmer spinal fusion and bone growth stimulators are being recalled because of the potential for bacterial contamination.
Some Zimmer spinal fusion and bone growth stimulators are being recalled because of the potential for bacterial contamination.
A Zimmer M/L Taper lawsuit claims that the hip implants are defective, with a high risk of corrosion, fretting and failure.
A new lawsuit claims that when the Zimmer M/L Taper Hip System is combined with the Versys cobalt-chromium femoral head, it becomes a defective product prone to fretting, corrosion and…
Zimmer M/L Taper hip component lawsuits filed in federal courts nationwide have been consolidated in the Southern District of New York for pretrial proceedings.
A Zimmer M/L Taper and VerSys hip implant lawsuit indicates that the components shed metal debris resulting in adverse tissue reactions and the need for revision surgery.
Zimmer faces a ZMR hip and Versys femoral head lawsuit over a case of metal blood poisoning linked to the hip replacement system.
Next month, the JPML will hear oral arguments over whether to consolidate all federal Zimmer M/L taper hip lawsuits for pretrial proceedings.
A Zimmer M/L/ Taper lawsuit indicates that a man had to have revision surgery in both hips after the devices corroded and shed metal debris that caused tissue reactions.
Zimmer says it opposes the creation of an MDL of hip replacement lawsuits involving its Zimmer M/L Taper system with Kinective and VerSys technologies.
The first M/L Zimmer Taper hip replacement system lawsuit is scheduled to go to trial on July 30 over claims that the implants are defective and prone to corrosion and…