Industry News
The latest medical device regulatory news, clinical trials, and market insights
NHS Leaders to Attend MEDICA 2025: Key Regulatory Insights for Medical Device Professionals
MEDICA 2025 is set to host a high-profile delegation from the UK’s National Health Service (NHS), offering critical insights into…
NHS Leaders to Attend MEDICA 2025: Key Regulatory Insights for Medical Device Professionals
MEDICA 2025 is set to host a high-profile delegation from the UK’s National Health Service (NHS), offering critical insights into…
Critical Updates on Medical Device Safety Alerts and Recalls from PMDA Japan
The Pharmaceuticals and Medical Devices Agency (PMDA) in Japan has released key updates on safety alerts, recalls, and related documentation…
Critical Updates on Medical Device Safety Alerts and Recalls from PMDA Japan
The Pharmaceuticals and Medical Devices Agency (PMDA) in Japan has released key updates on safety alerts, recalls, and related documentation…
Critical Updates on Medical Device Safety Alerts and Recalls from PMDA Japan
The Pharmaceuticals and Medical Devices Agency (PMDA) in Japan has released key updates on safety alerts, recalls, and related documentation…
Critical Updates on Medical Device Safety Alerts and Recalls from PMDA Japan
The Pharmaceuticals and Medical Devices Agency (PMDA) in Japan has released key updates on safety alerts, recalls, and related documentation…
Critical Updates on Medical Device Safety Alerts and Recalls from PMDA Japan
The Pharmaceuticals and Medical Devices Agency (PMDA) in Japan has released key updates on safety alerts, recalls, and related documentation…
Alcon Recalls Custom Pak Ophthalmic Procedure Packs Over Sterility Concerns
Alcon has initiated a voluntary recall involving certain Custom Pak Ophthalmic Procedure Packs due to concerns over potential sterility compromises.…
FDA Alert: Updated Instructions Issued for Calyxo CVAC Aspiration Systems
Calyxo Medical has issued an urgent update regarding the safe use of its CVAC Aspiration Systems. Health care providers and…
Critical FDA Alert: Fresenius Kabi Recalls Ivenix Infusion Pumps Due to Misassembly Risk
On January 10, 2026, the FDA issued an update regarding Fresenius Kabi’s recall of specific Ivenix Large Volume Pump (LVP)…
FDA Announces Critical Recall of Bravo CF Capsule Delivery Devices Due to Serious Safety Risks
Medtronic and its subsidiary Given Imaging Inc. have initiated a major recall of certain Bravo CF capsule delivery devices used…
Critical Recall of Novasight Hybrid Catheters Due to Potential Safety Risks
The FDA has announced a critical recall of the Novasight Hybrid catheters, manufactured by Conavi Medical Inc., due to safety…