42 results · 15ms · Sources: EU EUDAMED, US FDA

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X-Guide Handpiece Adaptor Sleeve 3, Model P010727

FDA Recall
Open, Classified ·X-NAV Technologies, LLC·Product code QRY·March 4, 2024

X-Guide Handpiece Adaptor Sleeve 1, Model P010701

FDA Recall
Open, Classified ·X-NAV Technologies, LLC·Product code QRY·March 4, 2024

X-Guide X-Mark Probe Tool -used for registering edentulous patients to the software or performing XMark registration. Catalog Number:P010673

FDA Recall
Open, Classified ·X-NAV Technologies, LLC·Product code QRY·September 28, 2022

ApexPro Telemetry Server System. Also identified as Modification To: ApexPro Telemetry System and ApexPro FH Telemetry System - Product Usage: These systems are typically deployed in sub acute care areas in hospitals or clinical sites where patient mobility can enhance the effectiveness of the medical procedures administered.

FDA Recall
Open, Classified ·GE Healthcare, LLC·Product code DSI·August 30, 2019

Dexcom G6 Glucose Receiver, SKUs (Part Number): STK-FM-001 (MT27408-1) & STK-FR-001 (MT27408-1)

FDA Recall
Open, Classified ·Dexcom, Inc.·Product code QBJ·May 12, 2025

Verigene Enteric Pathogens Nucleic Acid Test (EP) Model Number: 20-006-023

FDA Recall
Open, Classified ·Luminex Corporation·Product code OCC·October 30, 2020

Dexcom One Continuous Glucose Monitoring System, SKUs(Part Number): STK-DO-006 (MT27409-1), STK-DO-013 (MT27409-1), STK-DO-103 (MT27409-2), STK-DO-109 (MT27409-2)

FDA Recall
Open, Classified ·Dexcom, Inc.·Product code QBJ·May 12, 2025

Dexcom One+ Continuous Glucose Monitoring System, SKU(Part Number): STK-D7-013 (MT28285-1), STK-D7-014 (MT28285-1), STK-D7-103 (MT28285-2)

FDA Recall
Open, Classified ·Dexcom, Inc.·Product code QBJ·May 12, 2025

Colonoscope, Model Number PCF-H190L.

FDA Recall
Open, Classified ·Olympus Corporation of the Americas·Product code FDF·January 11, 2024

Colonoscope, Model Number PCF-H180AL.

FDA Recall
Open, Classified ·Olympus Corporation of the Americas·Product code NWB·January 11, 2024

Colonoscope, Model Number PCF-H190DL.

FDA Recall
Open, Classified ·Olympus Corporation of the Americas·Product code NWB·January 11, 2024

Colonoscope, Model Number CF-HQ190L.

FDA Recall
Open, Classified ·Olympus Corporation of the Americas·Product code FDF·January 11, 2024

Verigene Gram Negative Blood Culture Nucleic Acid Test v2 (BC-GNv2) Model Number: 20-006-026

FDA Recall
Open, Classified ·Luminex Corporation·Product code OCC·October 30, 2020

Verigene Gram Negative Blood Culture Nucleic Acid Test (BC-GN) Model Number: 20-006-021

FDA Recall
Open, Classified ·Luminex Corporation·Product code OCC·October 30, 2020

Verigene Clostridium difficile Nucleic Acid Test Kit (CDF) Model Number: 20-006-022

FDA Recall
Open, Classified ·Luminex Corporation·Product code OCC·October 30, 2020

Colonoscope, Model Number CF-HQ190I.

FDA Recall
Open, Classified ·Olympus Corporation of the Americas·Product code FDF·January 11, 2024

Colonoscope, Model Number PCF-Q180AL.

FDA Recall
Open, Classified ·Olympus Corporation of the Americas·Product code NWB·January 11, 2024

Verigene Gram-Positive Blood Culture Nucleic Acid Test (BC-GP) Model Number: 20-006-018

FDA Recall
Open, Classified ·Luminex Corporation·Product code OCC·October 30, 2020

Colonoscope, Model Number CF-Q180AL.

FDA Recall
Open, Classified ·Olympus Corporation of the Americas·Product code NWB·January 11, 2024

Colonoscope, Model Number PCF-H190TL.

FDA Recall
Open, Classified ·Olympus Corporation of the Americas·Product code NWB·January 11, 2024