FDA's new medical device quality management rules align U.S. standards with global requirements and give inspectors new ...
For most implants and other high-risk devices brought to market, manufacturers do nothing more than file some paperwork and ...
A fault in J&J MedTech’s CEREPAK detachable coils, used in intracranial aneurysm embolisation procedures, has been associated ...
Researchers at the company are trying to understand their A.I. system’s mind—examining its neurons, running it through ...
The global apheresis market has exhibited impressive growth, spurred by the increasing demand for plasma-derived products, advancements in apheresis technologies, and the rising prevalence of chronic ...
TransMedics Group, Inc. ("TransMedics") (Nasdaq: TMDX), a medical technology company that is transforming organ transplant therapy for patients with end-stage lung, heart, and liver failure, today ...
TransMedics Group, Inc. ("TransMedics") (Nasdaq: TMDX), a medical technology company that is transforming organ transplant ...
Medline recalls 4,300 blood culture kits due to packaging defects that could cause sterility issues with BD ChloraPrep ...
The manufacturer has identified that certain Abiomed heart pumps with differential pressure sensors have the potential to ...
FDA drug alerts in pulmonology, including drug approvals/warnings, vaccine approvals, medical device recalls/updates, and ...
The FDA has flagged J&J Medtech’s recall of its Cerepak detachable coils as Class I in the wake of one death and four serious ...
Medline recalls blood culture kits with packaging defects that may compromise sterility; customers must quarantine affected lots and follow ...
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