According to the U.S. Food and Drug Administration records, in an average year over 2,500 medical device recalls are issued in the United States. Some of these recalls simply require checking the ...
Tandem Diabetes Care issued an urgent medical device correction to upgrade the software of its Tandem Mobi insulin pumps that ...
A report published this week by the recall consulting group ExpertRecall analyzing the number of recalls in the regulated healthcare product sector shows that both pharmaceutical and medical device ...
The Food and Drug Administration lacks adequate staffing to oversee medical device recalls, according to a report released Friday by the U.S. Government Accountability Office. The report, which ...
The US Food and Drug Administration (FDA) saw more new recall events for class I medical devices in 2025 than it has in ...
Numerous medical devices sold in the United States are subject to active recalls. If you have a medical device that is subject to an active recall, it will be important to make sure you know what this ...
Medical device recalls are essential to patient safety, addressing critical issues in devices that may pose health risks. Here are some of the latest recalls reported to the FDA: AirLife/Vyaire ...
Hosted on MSN
Recall for medical device used by millions of Americans over malfunction that could lead to death
An urgent recall has gone out for a popular medical device used by millions of Americans with diabetes. The US Food and Drug Administration (FDA) has revealed that over two million blood glucose ...
The FDA has flagged four medical device recalls and alerts tied to risks that include device failure, oxygen complications and potential patient injury. Here are four recalls to know: 1. Angiographic ...
Medical device recalls are intended to act as a hard stop. When a defect is identified, products are removed from use, hospitals are notified, and patients are protected. At least, that is how the ...
This article originally appeared on ProPublica. The Food and Drug Administration rarely uses its authority to pull dangerous medical devices off the market and is so poorly staffed that it’s sometimes ...
Some results have been hidden because they may be inaccessible to you
Show inaccessible results