Posted inMedical Device
FDA Medline Bed Alert: How Overheating and Entrapment Hazards Arise in Powered Beds
The FDA Medline bed alert reports fire and entrapment hazards. How powered beds can fail and what the sources leave unanswered.
Posted inMedical Device
B. Braun Bloodline Alert: How a Missed Assembly Step Became an FDA Notice
The B. Braun Streamline Bloodline Set FDA alert traces a missed solvent step to a connector risk. What is known, and what the FDA is still reviewing.
Posted inMedical Device
BD Alaris Infusion Set FDA Alert: What Hospital Teams Should Check
The BD Alaris infusion set FDA alert asks hospitals to find affected Presource kits and manage low-rate infusions. The steps the FDA lists.
Posted inMedical Device
JAHA Study of EggNest Shielding Reports Lower Operator Radiation Doses in Cath Lab
A medical device radiation protection study of EggNest reports lower staff doses, per Egg Medical. The figures, caveats and open questions.
Posted inMedical Device
Vascular Closure Device Explained: What PerQseal Elite Changes
A vascular closure device seals the artery after catheter procedures. How Haemonetics’ PerQseal Elite patch works and what is still unproven.
Posted inMedical Device
Anaesthesia Workstation Manufacturer BPL Bets Big on Medec
Anaesthesia workstation manufacturer BPL takes a majority stake in Medec. What the products, patents and pipeline are, and what is undisclosed.
Posted inMedical Device
Indigenous Medical Devices India Get an ICMR Boost: Seven Centres
Indigenous medical devices India: ICMR picks seven research centres with up to Rs 15 crore each. What it means and what is still unknown.
Posted inMedical Device
Sahajanand Medical Technologies IPO Closes Today: Price Band, Issue Size and Business Explained
Sahajanand Medical Technologies IPO closes today: price band, offer-for-sale structure, allotment dates and the stent maker’s business.
Posted inMedical Device
FDA Flags Four Edwards Commander M Delivery System Lots After Death and Serious Injury Report
Edwards Lifesciences recall alert: FDA names four Commander M delivery system lots used with SAPIEN M3 after reported balloon ruptures. Lot numbers inside.
Posted inMedical Device
FDA Classifies AVID Medical IV Start Kit Lot 1658437 Recall as Class I Over Fungal Contamination Risk
AVID Medical recall lot number: only lot 1658437 is Class I. What FDA records show, where they differ, and what hospitals must do.