35 results · 12ms · Sources: EU EUDAMED, US FDA

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INFX-8000F Fluoroscopic X-Ray Systems

FDA Recall
Terminated ·Toshiba American Medical Systems Inc·Product code MBQ·December 29, 2017

CR NX Modality Workstation, Computed Radiography System (Software versions NX 1.0.2402 and NX 1.0.2405).

FDA Recall
Terminated ·AGFA Corp.·Product code MBQ·September 1, 2006

TheraSphere(R) YTTRIUM-90 CLASS MICROSPHERE INJECTION TheraSphere is indicated for radiation treatment or as a neoadjuvant to surgery or transplantation in patients with unresectable HCC who can have placement of appropriately positioned hepatic arterial catheters.

FDA Recall
Terminated ·Biocompatibles U.K., Ltd. Bortoli House Weydon Lane; Old Farnham Lane Farnham United Kingdom·Product code NAW·September 21, 2015

TheraSphere(R) YTTRIUM-90 CLASS MICROSPHERE INJECTION TheraSphere¿ is indicated for radiation treatment or as a neoadjuvant to surgery or transplantation in patients with unresectable HCC who can have placement of appropriately positioned hepatic arterial catheters.

FDA Enforcement
Class II ·Terminated·Biocompatibles U.K., Ltd.·October 19, 2016

Boston Scientific BLUE MAX" 20 Balloon Dilatation Catheter, UPN M001125420 (BMQ/7-4/5.8/40, 12-542), M001125630(BMQ/9-8/5.8/40, 12-563) Made in Ireland, Ballybrit Business Park, Galway, Ireland Recommended for Percutaneous Transluminal Angioplasty of the iliac, femoral and renal arteries and for the treatment of obstructive lesions of native or synthetic arteriovenous dialysis fistulae.

FDA Recall
Terminated ·Boston Scientific Corporation·Product code LIT·February 18, 2010

SHERPA NX ACTIVE GUIDING CATHETER, 6F MB1, .070", REF SA6MB1. for cardiovascular use

FDA Recall
Terminated ·Medtronic Vascular·Product code DQY·March 15, 2019

SHERPA NX ACTIVE GUIDING CATHETER, 6F, MB1, 90CM, 070", REF SA6MB1D. for cardiovascular use

FDA Recall
Terminated ·Medtronic Vascular·Product code DQY·March 15, 2019

SHERPA NX ACTIVE GUIDING CATHETER, 6F MB1 SH, .070", REF SA6MB1SH. for cardiovascular use

FDA Recall
Terminated ·Medtronic Vascular·Product code DQY·March 15, 2019

CATH. GUIDE 8F MB1 W/SH 110CM Coronary Guiding catheter designed to provide a pathway through which therapeutic and/or diagnostic devices are introduced into the coronary or peripheral vascular system. Product Code: Z28MB1SHA

FDA Recall
Terminated ·Medtronic, Inc.·Product code DQY·April 5, 2006

ReSolve Locking Drainage Catheters The ReSolve Locking Catheters are intended for percutaneous drainage of fluids from body cavities.

FDA Recall
Terminated ·Merit Medical Systems, Inc.·Product code GBQ·June 29, 2015

SS 3.5Mm Pellet Insertion Tray with large Gloves Catalog Number: B1352

FDA Recall
Terminated ·Busse Hospital Disposables, Inc.·Product code FBQ·February 22, 2022

SS 3.5MM Pellet Insertion Tray with Medium Gloves Catalog Number: B1354R1

FDA Recall
Terminated ·Busse Hospital Disposables, Inc.·Product code FBQ·February 22, 2022

SS 4.5MM Pellet Insertion Tray with Medium Gloves Catalog Number: B1365R1

FDA Recall
Terminated ·Busse Hospital Disposables, Inc.·Product code FBQ·February 22, 2022

4.5MM Pellet Insertion Tray with Medium Gloves Catalog Number: B1362

FDA Recall
Terminated ·Busse Hospital Disposables, Inc.·Product code FBQ·February 22, 2022

Male SS 4.5MM Pellet Insertion Tray Catalog Number: B9176R1

FDA Recall
Terminated ·Busse Hospital Disposables, Inc.·Product code FBQ·February 22, 2022

SS 4.5MM Pellet Insertion Tray Catalog Number: B9807

FDA Recall
Terminated ·Busse Hospital Disposables, Inc.·Product code FBQ·February 22, 2022

SS 3.5MM Diamond Tip Trocar - Large Gloves Catalog Number: B1547

FDA Recall
Terminated ·Busse Hospital Disposables, Inc.·Product code FBQ·February 22, 2022

SS 4.5MM DIAMOND TIP TROCAR WITH MEDIUM GLOVES Catalog Number: B1560

FDA Recall
Terminated ·Busse Hospital Disposables, Inc.·Product code FBQ·February 22, 2022

3.2MM Pellet Insertion Tray Catalog Number: B1144

FDA Recall
Terminated ·Busse Hospital Disposables, Inc.·Product code FBQ·February 22, 2022

Female SS 3.5MM Pellet Insertion Tray Catalog Number: B9175R1

FDA Recall
Terminated ·Busse Hospital Disposables, Inc.·Product code FBQ·February 22, 2022