85 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.

eCareCoordinator allows the customer to schedule patient tasks (i.e., take weight measurement, take blood pressure). For medical use by professional medical staff.

FDA Recall
Terminated ·Philips Visicu·Product code DRG·March 10, 2016

Sarns Cardioplegia Set CPLG BLD MP4 4:1 No recirculation, Item # 16010

FDA Recall
Terminated ·Terumo Cardiovascular Corporation·Product code DTR·June 8, 2010

Maquet Getinge-BEQ-TOP 49103 ECC Pack 0 No Bladder Material: 709000058

FDA Recall
Terminated ·Maquet Cardiovascular, LLC·Product code DWF·April 18, 2019

Terumo Cardiovascular Procedure Kit Custom CONDUCER/MP4 8:1 NO RECIRC. DOUBLE SPIKE P/N: 71032

FDA Recall
Terminated ·Terumo Cardiovascular Systems Corp·Product code DTR·June 8, 2010

Medline procedure packs containing Shenli syringes, labeled as follows: 1) DIALYSIS CATH ACCESS KIT, Pack Number DYNDA2516B ; 2) DIALYSIS PACK , Pack Number DYNJ36932A ; 3) DIALYSIS AV SHUNT #668229-V-LF, Pack Number DYNJ58502C ; 4) DIALYSIS ACCESS PACK, Pack Number DYNJ910121 ; 5) NO CATH DIALYSIS INSERTN TRAY , Pack Number PICCNC0028

FDA Recall
Open, Classified ·MEDLINE INDUSTRIES, LP Northfield·Product code PEV·April 8, 2024

AUTION HYBRID AU-4050

FDA Recall
Terminated ·Arkray Factory USA, Inc.·Product code KQO·May 3, 2019

Embrace Drill Tower, Standard/Lateral (25mm); Item Number: 645-081/63;

FDA Recall
Open, Classified ·Waldemar Link GmbH & Co. KG (Mfg Site) Ost Str. 4-10 Norderstedt Germany·Product code HTW·February 11, 2026

Embrace Drill Tower, Wedged (25mm); Item Number: 645-081/62;

FDA Recall
Open, Classified ·Waldemar Link GmbH & Co. KG (Mfg Site) Ost Str. 4-10 Norderstedt Germany·Product code HTW·February 11, 2026

SPII Model Lubinus, Hip Prosthesis Stem Standard Neck, cemented

FDA Recall
Open, Classified ·Waldemar Link GmbH & Co. KG (Mfg Site) Oststr. 4-10 Norderstedt Germany·Product code JDG·February 6, 2024

Embrace Drill Tower, Standard/Lateral (25mm)

FDA Recall
Open, Classified ·Waldemar Link GmbH & Co. KG (Mfg Site) Oststr. 4-10 Norderstedt Germany·Product code HTW·January 29, 2024

SPII Model Lubinus, Hip Prosthesis Stem XL Neck, cemented

FDA Recall
Open, Classified ·Waldemar Link GmbH & Co. KG (Mfg Site) Oststr. 4-10 Norderstedt Germany·Product code JDG·February 6, 2024

Embrace Drill Tower, Wedged (25mm)

FDA Recall
Open, Classified ·Waldemar Link GmbH & Co. KG (Mfg Site) Oststr. 4-10 Norderstedt Germany·Product code HTW·January 29, 2024

SPII Model Lubinus, Long Stem Prosthesis Standard Neck, cemented

FDA Recall
Open, Classified ·Waldemar Link GmbH & Co. KG (Mfg Site) Oststr. 4-10 Norderstedt Germany·Product code JDG·February 6, 2024

SPII Model Lubinus, Long Stem Prosthesis XL Neck, cemented

FDA Recall
Open, Classified ·Waldemar Link GmbH & Co. KG (Mfg Site) Oststr. 4-10 Norderstedt Germany·Product code JDG·February 6, 2024

Colpassist Vaginal Positioning Device - Product Usage: intended for use in general gynecological surgery to assist in the positioning and manipulation of the vagina during the procedure. Material No. M0068318210

FDA Recall
Open, Classified ·Boston Scientific Corporation·Product code KOH·April 15, 2021

Artis icono biplane with software VE20C-diagnostic imaging angiography system Model: 11327600

FDA Recall
Terminated ·Siemens Medical Solutions USA, Inc·Product code OWB·October 12, 2021

Artis icono floor with software VE20C-diagnostic imaging angiography system Model: 11327700

FDA Recall
Terminated ·Siemens Medical Solutions USA, Inc·Product code OWB·October 12, 2021

Beckman Coulter, IVD, REF: OSR61171, IgA, 4 x 14 mL R1, 4 x 11 mL R2

FDA Recall
Open, Classified ·Beckman Coulter Inc.·Product code CFN·July 12, 2023

Artis pheno with software VE20C- diagnostic imaging angiography system Model: 10849000

FDA Recall
Terminated ·Siemens Medical Solutions USA, Inc·Product code OWB·October 12, 2021

Cardiosave Hybrid Intra-Aortic Balloon Pumps (IABP), Model Number 0998-00-0800-55, Part Number 0998-00-0800-XX

FDA Recall
Open, Classified ·Datascope Corp.·Product code DSP·May 4, 2023