115 results · 31ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

Medica Capillary Tubes; EasyBloodGas/EasyStat Capillary Tube Kit.

FDA Recall
Open, Classified ·Medica Corporation·Product code CEM·December 31, 2025

iCast Covered Stent, 6MMx16MMx120CM, Model Number 42616

FDA Recall
Open, Classified ·Atrium Medical Corporation·Product code PRL·September 9, 2024

Ocean Water Seal Chest Drains (Ocean): Products REF Number Product Name (1)2002-000 DRAIN, OCEAN SINGLE W/AC,S; (2)2002-040 DRAIN, OCEAN SINGLE,PEDI CONNECTOR; (3)2002-100 DRAIN, OCEAN SINGLE W/AC; (4)2002-300 DRAIN, OCEAN SINGLE W/S; (5) 2002-400 DRAIN, OCEAN SINGLE ; (6)2012-320 DRAIN, OCEAN PEDI W/S; (7)2050-000 DRAIN, OCEAN BRU W/AC,S

FDA Recall
Open, Classified ·Atrium Medical Corporation·Product code CAC·September 18, 2023

FLIXENE, 4-7X30, 2GDS, GWT-GW. Double-Ended Slider GDS. Vascular graft

FDA Recall
Open, Classified ·Atrium Medical Corporation·Product code DSY·May 3, 2024

FLIXENE, 7X50, 1GDS, GW. Single-Ended Slider GDS. Vascular graft

FDA Recall
Open, Classified ·Atrium Medical Corporation·Product code DSY·May 3, 2024

ADVANTA VXT, 6X70, 1GDS, NH, STR-SW. Single-Ended Slider. Vascular graft

FDA Recall
Open, Classified ·Atrium Medical Corporation·Product code DSY·May 3, 2024

FLIXENE, 7X30, 1GDS, GW. Single-Ended Slider GDS. Vascular graft

FDA Recall
Open, Classified ·Atrium Medical Corporation·Product code DSY·May 3, 2024

ADVANTA VXT, 8X50, 1GDS, NH, STR-SW. Single-Ended Slider. Vascular graft

FDA Recall
Open, Classified ·Atrium Medical Corporation·Product code DSY·May 3, 2024

FLIXENE, 7X80, 1GDS, GW. Single-Ended Slider GDS. Vascular graft

FDA Recall
Open, Classified ·Atrium Medical Corporation·Product code DSY·May 3, 2024

ADVANTA VXT, 4-7X45, 1GDS, NH, TPR-SW. Single-Ended Slider GDS. Vascular graft

FDA Recall
Open, Classified ·Atrium Medical Corporation·Product code DYF·May 3, 2024

ADVANTA VXT, 8X70, 1GDS, FH, STR-TW. Single-Ended Slider GDS. Vascular graft

FDA Recall
Open, Classified ·Atrium Medical Corporation·Product code DSY·May 3, 2024

ADVANTA VXT, 7X70, 1GDS, NH, STR-SW. Single-Ended Slider. Vascular graft

FDA Recall
Open, Classified ·Atrium Medical Corporation·Product code DSY·May 3, 2024

FLIXENE, 4-7X45, 2GDS, GWT. Double-Ended Slider GDS. Vascular graft

FDA Recall
Open, Classified ·Atrium Medical Corporation·Product code DSY·May 3, 2024

FLIXENE, 6X40, 1GDS, GW. Single-Ended Slider GDS. Vascular graft

FDA Recall
Open, Classified ·Atrium Medical Corporation·Product code DSY·May 3, 2024

ADVANTA VXT, 6X50, 1GDS, FH, STR-TW. Single-Ended Slider GDS. Vascular graft

FDA Recall
Open, Classified ·Atrium Medical Corporation·Product code DSY·May 3, 2024

Atrium Pneumostat Chest Drain Valve, Part Number 16100

FDA Recall
Open, Classified ·Atrium Medical Corporation·Product code KDQ·August 26, 2021

Brand Name: ZOLL Product Name: Powerheart G5 AED Model/Catalog Number: (1) G5S-01C, (2) G5S-02C, (3) G5S-10C, (4) G5S-11C; Software Version: NA Product Description: The Powerheart G5 automated external defibrillator (AED) is designed for treating life-threatening heart beat irregularities, such as ventricular fibrillation, that cause Sudden Cardiac Arrest (SCA). There are two models available fully automatic and semi-automatic. After the defibrillations pads are applied to the patient, the fully automatic model evaluates the heart rhythm and, if a shockable rhythm is detected, delivers a shock without any rescuer assistance. The semi-automatic model evaluates the heart rhythm and requires the rescuer to press the shock button if a shockable rhythm is detected. Both models have voice and text instructions that guide the rescuer through the entire defibrillation process. Note: Not all configurations described in this document are available in all areas.

FDA Recall
Open, Classified ·ZOLL Medical Corporation·Product code MKJ·February 13, 2025

Atrium Firm PVC Thoracic Catheter 36FR Straight, part number 15036.

FDA Recall
Open, Classified ·Atrium Medical Corporation·Product code GBZ·September 29, 2023

ADVANTA VXT, 8X40, 1GDS, NH, STR-SW. Single-Ended Slider. Vascular graft

FDA Recall
Open, Classified ·Atrium Medical Corporation·Product code DSY·May 3, 2024

FLIXENE, 4-6X45, 2GDS, GWT-GW. Double-Ended Slider GDS. Vascular graft

FDA Recall
Open, Classified ·Atrium Medical Corporation·Product code DSY·May 3, 2024