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ANSM Drug & Device Safety Alert: Endoscopic Clip Device

The French ANSM has issued a safety information notice regarding a recall of specific lots of the Instinct Plus endoscopic clip device by Wilson-Cook Medical, Inc. This action follows a previous safety alert and is registered under ANSM reference R2606331.

Philips Respironics BiPAP A40 Pro Ventilator - Discontinuation and Safety Alert

Philips Respironics is discontinuing the BiPAP A40 Pro ventilator globally due to an internal oxygen sensor defect causing false alarms. The company offers patients options for continued care, including device replacement or partial reimbursement. Healthcare providers must inform affected patients of these options.

ANSM Safety Information for Hemostasis Reagent STA NeoPTimal 5

The French ANSM has issued a safety information notice regarding the Hemostasis Reagent STA NeoPTimal 5, manufactured by Diagnostica Stago. Affected users have been notified directly by the company, and the action is registered under ANSM number R2607353.

ANSM Safety Recall: Autoimmunity IDS SS-A/Ro Reagent

The French ANSM has issued a safety recall (R2532493) for a specific lot of the Autoimmunity IDS SS-A/Ro reagent manufactured by Immunodiagnostic Systems (IDS). Laboratories using this reagent have been notified directly by the manufacturer.

Leksell Vantage stereotactic system safety information

The French ANSM has issued a safety notice regarding the Leksell Vantage stereotactic system by Elekta Ltd. This action, registered under number R2607991, is based on a safety action implemented by the manufacturer. Affected healthcare facilities have been notified.

Philips Spectral CT Scanner Software Safety Alert

The French ANSM has issued a safety alert (R2607608) regarding Philips Spectral CT scanner systems with software version 5.1.X. Healthcare facilities using these devices have been notified of a security action initiated by Philips Medical Systems BV.

Health Commissioner Statement on Court Ruling and Vaccine Science

New York State Health Commissioner Dr. James McDonald issued a statement on a federal judge's ruling concerning the Advisory Committee on Immunization Practices (ACIP). The statement reaffirms the department's commitment to vaccine science and protection against preventable diseases.

FDA: Dialysis Tubing Sets Recalled Due to Dislodging, Updated Instructions

The FDA is alerting healthcare providers about a recall of Vantive dialysis tubing sets due to potential dislodging of the deaeration chamber. Updated instructions for use have been issued to mitigate risks, emphasizing monitoring the chamber during therapy. This is a correction and does not involve removing the devices from use or sale.

DEA Seattle Fentanyl Enforcement and Awareness Initiative

The DEA's Seattle Division is launching a "Fentanyl-Free America" initiative in the Pacific Northwest, focusing on increased enforcement, education, and awareness. This initiative aims to combat the fentanyl crisis through collaborative efforts.

MHRA Field Safety Notices for Medical Devices

The MHRA has published a list of Field Safety Notices (FSNs) for medical devices issued between March 9-13, 2026. These notices are for informational purposes, and recipients are advised to act on any FSN received from a manufacturer.