8 results · 29ms · Sources: EU EUDAMED, US FDA

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ENDOTAK RELIANCE G/SG with 4-SITE Connector, transvenous defibrillation lead, Permanent Defibrillator Electrodes; Model Nos. 0282, 0283, 0285, 0286, 0292, 0293, 0295, 0296

FDA Recall
Open, Classified ·Boston Scientific Corporation·Product code NVY·July 24, 2025

ENDOTAK RELIANCE G/SG, transvenous defibrillation lead, implantable cardioverter defibrillator (non-CRT); Model Nos. 0160, 0161, 0162, 0163, 0164, 0165, 0166, 0167, 0170, 0171, o182, 0173, 0174, 0175, 0176, 0177, 0180, 0182, 0183, 0184, 0185, 0186, 0187

FDA Recall
Open, Classified ·Boston Scientific Corporation·Product code LWS·July 24, 2025

VIDAS CLINICAL VIDAS LISTERIA 60T, CATALOG 30700

FDA Recall
Open, Classified ·Biomerieux Inc·Product code GSG·November 9, 2022

ASG-001; Ultrasound gel

FDA Recall
Open, Classified ·Advance Medical Designs, Inc.·Product code MUI·July 7, 2023

CoViPoint COVID test kit (MultiPLEX/Direct) Kit Item Numbers: BC-DK0200; BM-AD4K0200 BM-ADK0200 BM-CDK0200 BM-CFDK0200 BM-D4K0200 BM-DK0200 BM-DK0600 BM-DK0800 BM-DK1200 BM-DK1400 BM-DK1800

FDA Recall
Open, Classified ·GS Biomark LLC·Product code QJR·August 8, 2022

daVinci XI Sureform 60 reload, 60 mm Green 6- Row, 4.6 mm, REF 48360G-08, UDI: 00886874113844, Rx Only, Sterile EO - Product Usage: are intended to be used with da Vinci Surgical Systems for resection, transection, and, or creation of anastomoses in General, Thoracic, Gynecologic, Urologic, and Pediatric surgery.

FDA Recall
Open, Classified ·Intuitive Surgical, Inc.·Product code GAG·July 1, 2019

daVinci XI Sureform 60 Reload, 60 mm black 6-Row 4.6 mm, Ref: 48360T-08 , UDI: 00886874113851, Rx only, SterileEO - Product Usage: are intended to be used with da Vinci Surgical Systems for resection, transection, and, or creation of anastomoses in General, Thoracic, Gynecologic, Urologic, and Pediatric surgery.

FDA Recall
Open, Classified ·Intuitive Surgical, Inc.·Product code GAG·July 1, 2019

EEA Autosuture Circular Stapler with DST Series Technology, 25mm. Model Numbers EEA25, EEAXL25, EEA2535, and EEAXL2535.

FDA Recall
Open, Classified ·Product code GAG·May 13, 2022