224 results · 22ms · 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.

Cobalt Implantable Cardioverter Defibrillators with Cardiac Resynchronization Therapy (CRT-D)

FDA Recall
Open, Classified ·Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)·Product code NIK·November 5, 2020

SUCTION / ANTICOAGULATION ASSEMBLY (a) BTC93 (b) BTC98 Suction and Anticoagulation assemblies are indicated for use with an autotransfusion system between the suction tip and reservoir.

FDA Recall
Open, Classified ·Medtronic Perfusion Systems·Product code CAC·November 27, 2018

RESERVOIR "Y" ADAPTER, (a) BT920 (b) BT926 Suction and Anticoagulation assemblies are indicated for use with an autotransfusion system between the suction tip and reservoir.

FDA Recall
Open, Classified ·Medtronic Perfusion Systems·Product code CAC·November 27, 2018

smith&nephew EVOS CONDYLAR MEDIAL DISTAL FEMUR PLATE, R, 5H, 115MM, REF 72573202

FDA Recall
Open, Classified ·Smith & Nephew, Inc.·Product code HRS·November 1, 2021

smith&Nephew EVOS MEDIAL DISTAL FEMUR PLATE, L, 5H, 90MM, REF 72573101

FDA Recall
Open, Classified ·Smith & Nephew, Inc.·Product code HRS·November 1, 2021

smith&nephew EVOS MEDIAL DISTAL FEMUR PLATE, R, 5H, 90MM, REF 72573201

FDA Recall
Open, Classified ·Smith & Nephew, Inc.·Product code HRS·November 1, 2021

smith&nephew EVOS CONDYLAR MEDIAL DISTAL FEMUR PLATE, L, 5H, 115MM, REF 72573102

FDA Recall
Open, Classified ·Smith & Nephew, Inc.·Product code HRS·November 1, 2021

QIAcube Connect MDx, Model No. 9003070

FDA Recall
Open, Classified ·Qiagen Sciences LLC·Product code JJH·November 21, 2021

VITEK 2 REAGENT AST-XN15 TEST KIT 20 CARDS, CATALOG 423829

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

VIDAS CLINICALVIDAS VARICEL. ZOSTER IGG 60 T, CATALOG 30217

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

ETEST CLINICAL ETEST MEROPENEM MP M100 US, CATALOG 423786

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

ETEST CLINICAL CEFTRIAXONE TX 32 US S30, CATALOG 412302

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

ETEST CLINICAL COLISTIN CO 256 US B100, CATALOG 537348

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

ETEST CLINICAL BENZYLPENICIL PG 256 US S30, CATALOG 412262

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

PPM LOMBARD PRODUCTS T PHOSPHATE BUFFERSTERILE 20X9ML, CATALOG T8035

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

PPM CLINICAL CRAPONNE CLINICAL CHROMID CANDIDA 20 PLATES, CATALOG 43631

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

ETEST CLINICAL ERTAPENEM ETP 32 US S30, CATALOG 412331

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

ETEST CLINICAL AMOXI/CLAV 2/1 XL 256 US S30, CATALOG 412240

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

PPM LOMBARD PRODUCTS CT&IR&DB-TSA + L & P80 10PLT, CATALOG C6045-IR

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

VIDAS CLINICAL VIDAS HCG 60 TESTS, CATALOG 30405-01

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