The company began the recall after receiving four field complaints about tip separation before and during use.

Medical device recalls are essential to patient safety, addressing critical issues in devices that may pose health risks. Here are some of the most recent recalls reported to the FDA: Zoll recalls ...

The Food and Drug Administration published an early alert for the recall on Tuesday. No deaths have been associated with the ...

The medical cannula market is experiencing consistent growth, driven by the global demand for advanced medical devices and ...

BSX also posted solid first-quarter 2025 earnings, with adjusted EPS of $0.75 and sales worth $4.66 billion, both beating expectations on the back of cardiovascular and medical-surgical divisions.

Who's cleaning medical equipment? The answer affects patient flow Recommended Live Webinar on Aug 13, 2025 12:00 PM - 1:00 PM CDT ...

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 ...

Master effective recall management with the two day FDA Recalls Masterclass course. Understand FDA recall authority, develop effective recall strategies, and improve compliance. Learn to identify root ...

The recall affects devices under the product name Shiley Adult Flexible Tracheostomy Tube with TaperGuard Cuff Reusable Inner Cannula, with UDI numbers A8845212054401, 20884521205441, and ...

Smiths Medical has not reported any serious injuries or deaths related to these issues, but the FDA determined there is a risk of harm. The devices are staying on the market.