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

Ensuring the safety and quality of pharmaceuticals, such as blood products, vaccines, recombinant proteins, and monoclonal antibodies, is essential. Endotoxins act as a hidden ‘time bomb’ in these ...

Helping Products Stay on the Market Without Issues Statistics indicate that approximately 4,500 medical devices and drugs get taken off the market owing to recalls. Just as managerial reviews of ISO ...

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 FDA issued a notice identifying a high-risk device issue associated with a Medtronic recall of Bravo CF capsule delivery ...

Teva pharmaceuticals has issued a voluntary recall of one lot of its reflux medication after discovering that bottles contained tablets of a drug used to treat fluid retention. The recall affects lot ...

The global medical device packaging market is expected to be grow from an estimated $12,409.8 million to $20,914 million in 2033, surging at a stable compound annual growth rate (CAGR) of 6.1% over ...

Major changes to the regulation of medical devices in Great Britain have come into effect, including a requirement that manufacturers carry out stricter post-marketing surveillance (PMS) of their ...

The new European Medical Device Regulation (EU MDR) and its implementation are causing delays and complexities for foreign companies looking to place or maintain devices on the EU market, and, as ...

Efficient scheduling is the backbone of a thriving dermatology practice. With increasing demand for streamlined operations, ...