FDA Launches Pilot to Improve Timeliness of Medical Device Recall Alerts
The pilot aims to minimize the time between the FDA’s initial awareness of and public notification of potentially high-risk medical device removals or corrections.
The pilot aims to minimize the time between the FDA’s initial awareness of and public notification of potentially high-risk medical device removals or corrections.
The FDA cautions health providers to stop using the Quidel Triage Cardiac Panel due to potential inaccuracies in troponin levels. Alternatives are recommended to ensure accurate diagnoses for myocardial infarction.