-
BioPro Femoral Head (Metal 22, 28, 32, 36, 40) cobalt chromium and ceramic… recall
FDA
· BioPro, Inc. · Class II
-
ECHELON LINEAR Cutters Reload 80 mm Blue, intended for transection… recall
FDA
· Ethicon Endo Surgery, LLC · Class II
-
XERF EFFECTOR 60. Electrosurgical unit recall
FDA
· Lutronic Corporation · Class II
-
ARVIS Product Name: ARVIS" Shoulder Model recall
FDA
· Kico Knee Innovation Company · Class II
-
LGX Preconnect with TENACIO Pump with InhibiZone recall
FDA
· Boston Scientific Corporation · Class II
-
CXR Preconnect with TENACIO Pump with InhibiZone recall
FDA
· Boston Scientific Corporation · Class II
-
CX Preconnect with TENACIO Pump with InhibiZone recall
FDA
· Boston Scientific Corporation · Class II
-
LGX Preconnect with TENACIO Pump without InhibiZone recall
FDA
· Boston Scientific Corporation · Class II
-
CX Preconnect with TENACIO Pump without InhibiZone recall
FDA
· Boston Scientific Corporation · Class II
-
TENACIO Pump without InhibiZone recall
FDA
· Boston Scientific Corporation · Class II
-
TENACIO Pump with InhibiZone recall
FDA
· Boston Scientific Corporation · Class II
-
Medline Adult Anesthesia Set recall
FDA
· Medline Industries, LP · Class II
-
C-Rex UNO Microinterventional Goniotomy Instrument recall
FDA
· Iantrek Inc. · Class II
-
Cyclopen Microinterventional Cyclodialysis System recall
FDA
· Iantrek Inc. · Class II
-
FERNO POWER X2 POWERED AMBULANCE COT, Model recall
FDA
· Ferno-Washington Inc · Class II
-
The failure occurs if a user on the Omnipod 5 iOS application selects and… recall
FDA
· Insulet Corporation · Class II
-
Neuroguard IEP 3 in 1 Carotid Stent and Post-Dilation Balloon System with… recall
FDA
· Contego Medical, Inc · Class II
-
Flow Re-Direction Endoluminal Devices: FRED 27 recall
FDA
· Microvention Inc. · Class II
-
NutraGlide Nasal Feeding Tube with Stylet and ENFit, 5 F - 8 F x 90 recall
FDA
· Applied Medical Technology Inc · Class II
-
NutraGlide Nasal Feeding Tube with Stylet and ENFit, 5 F - 8 F x 55 recall
FDA
· Applied Medical Technology Inc · Class II
-
NutraGlide Nasal Feeding Tube with Stylet and ENFit, 5 F - 6 F x 90 recall
FDA
· Applied Medical Technology Inc · Class II
-
NutraGlide Nasal Feeding Tube with Stylet and ENFit, 5 F - 6 F x 55 recall
FDA
· Applied Medical Technology Inc · Class II
-
Design Options, PERIFIX FX Epidural Anesthesia Tray recall
FDA
· B Braun Medical Inc · Class II
-
Combined Spinal and Epidural Anesthesia Tray 2, PERIFIX 17 Ga recall
FDA
· B Braun Medical Inc · Class II
-
Design Options, Pain Management Tray recall
FDA
· B Braun Medical Inc · Class II
-
Combined Spinal and Epidural Anesthesia Tray, PERIFIX 17 Ga recall
FDA
· B Braun Medical Inc · Class II
-
ESPOCAN Combined Spinal and Epidural Anesthesia Tray, ESPOCAN 17 Ga recall
FDA
· B Braun Medical Inc · Class II
-
PERIFIX FX Continuous Epidural Anesthesia Set… recall
FDA
· B Braun Medical Inc · Class II
-
PERIFIX FX Continuous Epidural Anesthesia Tray, PERIFIX 17 Ga recall
FDA
· B Braun Medical Inc · Class II
-
PERIFIX FX Continuous Epidural Anesthesia Tray, PERIFIX 17 Ga recall
FDA
· B Braun Medical Inc · Class II
-
PERIFIX FX Continuous Epidural Anesthesia Tray, 17 Ga recall
FDA
· B Braun Medical Inc · Class II
-
PERIFIX FX Continuous Epidural Anesthesia Tray with PERIFIX 17 Ga recall
FDA
· B Braun Medical Inc · Class II
-
PERIFIX FX Continuous Epidural Anesthesia Tray with PERIFIX 17 Ga recall
FDA
· B Braun Medical Inc · Class II
-
PERIFIX FX Continuous Epidural Anesthesia Tray with PERIFIX 17 Ga recall
FDA
· B Braun Medical Inc · Class II
-
PERIFIX FX Continuous Epidural Anesthesia Tray with PERIFIX 17 Ga recall
FDA
· B Braun Medical Inc · Class II
-
FlexLab X (FXX) System recall
FDA
· Inpeco S.A. · Class II
-
FlexLab (FLX) System recall
FDA
· Inpeco S.A. · Class II
-
Artegraft Collagen Vascular Graft recall
FDA
· LeMaitre Vascular, Inc. · Class II
-
SYNCHRON Systems Phosphorus (PHOSm) Reagent recall
FDA
· Beckman Coulter, Inc. · Class II
-
AW Server 2.0, AW Server 3.0, AW Server 3.1, AW Server 3.2 recall
FDA
· GE Medical Systems SCS · Class II
-
FDR Visionary Suite, CH-200 Model/Version Numbers: (1) 566-16130-23… recall
FDA
· FUJIFILM Healthcare Americas Corporation · Class II
-
Optiflux¿ High Flux E-beam Dialyzer Model Numbers: (1) 0500316E OPTIFLUX… recall
FDA
· Fresenius Medical Care Holdings, Inc. · Class II
-
EverPatch+ recall
FDA
· Corneat Vision, Ltd. · Class II
-
CorNeat EverPatch recall
FDA
· Corneat Vision, Ltd. · Class II
-
ClariTEE Miniaturized TEE probe recall
FDA
· ImaCor Inc. · Class II
-
This device is a digital radiography/fluoroscopy system used in a… recall
FDA
· Canon Medical System, USA, INC. · Class II
-
Ashvins variant HEYEX 2 / HEYEX PACS. Software Version: Version 2.6.0… recall
FDA
· MedicalCommunications GmbH · Class II
-
Argus PB-3000, Reference Numbers: 1A.701307,3.921002, 3.921030,3.921031… recall
FDA
· Schiller, Ag · Class II
-
VITEK¿ 2 Gram-negative AST Test Kits (Cards) containing Colistin… recall
FDA
· Biomerieux Inc · Class II
-
1. EXETER V40 STEM 44MM NO 2, Model recall
FDA
· Howmedica Osteonics Corp. · Class II
-
ZAP-X Radiosurgery System, Model: 300150 recall
FDA
· Zap Surgical Systems · Class II
-
Venclose digiRF Generators, Model VCRFG1, with software 3.35 designed to… recall
FDA
· Bard Peripheral Vascular Inc · Class II
-
JUNCTIONAL EMERGENCY TREATMENT TOOL (JETT) recall
FDA
· North American Rescue LLC. · Class II
-
GORE ACUSEAL Vascular Graft recall
FDA
· W L Gore & Associates, Inc. · Class II
-
Artegraft Collagen Vascular Grafts Model Numbers: (1) AG 616, (2) AG 630… recall
FDA
· LeMaitre Vascular, Inc. · Class II
-
Medtronic, Simplera Sensor recall
FDA
· Medtronic MiniMed, Inc. · Class II
-
DxC 500 AU Module w/ISE, DxC 500i, With ISE recall
FDA
· Beckman Coulter, Inc. · Class II
-
Change Healthcare Radiology Solutions software version 14.2.2 recall
FDA
· Change Healthcare Canada Company · Class II
-
AESCULAP ELAN 4 FIXED DURAGUARD LONG. Model Number: GB943R recall
FDA
· Aesculap AG · Class II
-
AESCULAP ELAN 4 FIXED DURAGUARD STANDARD. Model Number: GB942R recall
FDA
· Aesculap AG · Class II