Tag Archives: Bone Implant

Bone Matrix Tuberculosis Outbreak Leads to CDC Calls for Better Donor Screening

January 09, 2024 By: Katherine McDaniel

A tuberculosis outbreak was linked to Aziyo Biologics earlier this year, resulting in at least five infections and two deaths; which is the second such bone matrix tuberculosis outbreak linked to the company's products.
Bone Matrix Graft Products Linked to Tuberculosis Risks, FDA Warns

September 13, 2023 By: Irvin Jackson

The FDA is calling for more stringent screening of bone matrix tissue donors in light of repeated tuberculosis outbreaks among bone graft patients
FDA Issues Letter To Doctors About Issues with NuVasive Precice Limb-Lengthening Devices

June 29, 2023 By: Martha Garcia

Prior warnings and recalls of the limb-lengthening implants have raised concerns about biocompatibility problems, leading the FDA to warn doctors to remove the devices after one year.
Mechanical Failures, Biocompatibility Problems with NuVasive MAGEC System Implants Lead To FDA Warning

July 19, 2021 By: Russell Maas
FDA Warns of Biocompatibility Risks With NuVasive Specialized Orthopedics’ Precice devices

July 12, 2021 By: Russell Maas

Philips CPAP Injury Lawsuits To Be Selected For Potential Bellwether Trials in October 2024 (Posted 3 days ago)

A scheduling order issued by a federal judge calls for parties to have a plan to select potential Philips CPAP injury lawsuit bellwether selections by the end of October.

Lawsuits Over Ozempic, Wegovy, Mounjaro and Other GLP1-RA Drugs May Hinge on Label Warnings (Posted 6 days ago)

Parties involved in GLP-1 RA injury lawsuits have filed position papers staking out their arguments over the adequacy of Ozempic, Mounjaro and Wegovy label warnings.

MDL Judge Dismisses Four Paraquat Bellwether Cases, After Excluding Plaintiffs' Expert Witness From Testifying at Trial (Posted 7 days ago)

A federal judge has dismissed four Paraquat bellwether trial cases after rejecting expert witness testimony necessary to establish that their Parkinson's disease was caused by the controversial weed killer.

Tag Archives: Bone Implant

Bone Matrix Tuberculosis Outbreak Leads to CDC Calls for Better Donor Screening

Bone Matrix Graft Products Linked to Tuberculosis Risks, FDA Warns

FDA Issues Letter To Doctors About Issues with NuVasive Precice Limb-Lengthening Devices

Mechanical Failures, Biocompatibility Problems with NuVasive MAGEC System Implants Lead To FDA Warning

FDA Warns of Biocompatibility Risks With NuVasive Specialized Orthopedics’ Precice devices

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