Industry Updates
- Australia’s TGA Sues Medtronic for Unlawful Supply of Bone Graft Kit
- FDA, ECRI Release First Reports on Safety of Materials Used in Implantable Devices
- Australia Reports Progress in Implementing Medical Device Reforms
- Shortages, Other COVID-19 Impacts to Affect Device Makers Into Next Year
- EU Expert Panels to Review High-Risk IVDs
- Elekta Instrument AB Recalls Disposable Biopsy Needle Kit for Leksell Stereotactic System for Possibly Containing Microscopic Stainless Steel Debris on the Inside of the Biopsy Needle
- 2024 Medical Device Recalls
- FDA Encourages the Public to Follow Established Choking Rescue Protocols: FDA Safety Communication
- InfuTronix, LLC Recalls Nimbus and Nimbus II Infusion Pump Systems for Multiple Device Failures That May Cause Severe Injury and Death
- Outset Medical, Inc. Recalls Certain Tablo Hemodialysis Systems for Risk of Patient Exposure to Higher Than Allowable Levels of Toxic Compound NDL-PCBAs
- New Creatinine- and Cystatin C–Based Equations to Estimate GFR without Race
- Time to Eliminate Health Care Disparities in the Estimation of Kidney Function
- Uncomfortable Truths — What Covid-19 Has Revealed about Chronic-Disease Care in America
- The 2021 Reauthorization of CAPTA — Letting Public Health Lead
- Point-of-Care Ultrasonography
- Acute Promyelocytic Leukemia
- Journal Voices in the Civil Rights Era — New Horizons and Limits in Medical Publishing
- The Quest for Transformative Tools to Eradicate Malaria
- Subcutaneous Administration of a Monoclonal Antibody to Prevent Malaria
- Oral Simnotrelvir for Adult Patients with Mild-to-Moderate Covid-19