FDA Warns of High Rate of Stryker STAR Ankle Implants Breaking
The FDA warns Stryker STAR Ankle Replacement implants appear to have a higher-than-expected risk of failures, often resulting in the need for revision surgery.
The FDA warns Stryker STAR Ankle Replacement implants appear to have a higher-than-expected risk of failures, often resulting in the need for revision surgery.
A petition filed in New Jersey courts seeks to consolidate all Stryker Tritanium Acetabular Cup hip system lawsuits filed in that state before one judge for pretrial proceedings.
Patients and doctors are being warned about a risk of problems with Stryker STAR Ankle Replacements, which may fracture or break at a higher rate than expected, resulting in initial…
A hip implant lawsuit claims the Stryker Trident Tritanium Acetabular Cup is defectively designed and prone to failure, resulting in a Texas woman needing revision surgery after just four years.
Stryker is warning of potential problems with its Lifepak-15 defibrillators that could lead to them locking up, and has been linked to at least six deaths.
Parties have reached a potential settlement agreement on resolving some Stryker LFit V40 hip component system lawsuits.
A hip implant lawsuit filed against Stryker indicates that its Secur-Fit and C-Taper Fit hip components are prone to fretting, corrosion and failure.
A knee replacement system lawsuit claims that the Restoris MCK system is defective, resulting in loosening and failure.
A new warning indicates that some Stryker LFit V40 femoral head hip system components may be prone to dissociation, which could lead to dislocation, pain and the need for revision…
A federal judge has called for the selection of 18 Stryker LFit V40 hip lawsuits to comprise an initial discovery pool, from which the first bellwether cases will be selected…