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NavPro ONE Device with touchscreen

FDA UDI
PATH medical GmbH·04260223143311·NavPRO One branded Sentiero Advanced

NP "O" Series OR Pad - Foam Mattress Family

FDA UDI
SIZEWISE RENTALS, L.L.C.·00845699002900·

BARD POWERMIDLINE CATHETER (4F) (SINGLE-LUMEN) (20CM)

FDA Adverse Event
Malfunction ·C.R. BARD, INC. (BASD) -3006260740·Product code PND·May 13, 2022

PRO-LINE CT

FDA Adverse Event
Malfunction ·MEDICAL COMPONENTS, INC.·Product code LJS·August 23, 2024

ALARIS

FDA Adverse Event
Injury ·CARE FUSION·Product code FRN·March 14, 2014

PROCLAIM¿ 5 ELITE IMPLANTABLE PULSE GENERATOR

FDA Adverse Event
Injury ·ST. JUDE MEDICAL - NEUROMODULATION (PUERTO RICO, LLC)·Product code LGW·October 3, 2022

MINI ONE® BALLOON BUTTON

FDA Adverse Event
Injury ·APPLIED MEDICAL TECHNOLOGY, INC.·Product code KNT·January 19, 2017

ALARIS

FDA Adverse Event
Malfunction ·ALARIS MEDICAL SYSTEMS INC·Product code FPA·March 7, 2005

POWERED 60 ECHELON +, 440MM SHAFT

FDA Adverse Event
Injury ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·September 22, 2021

POWERED 60 ECHELON +, 440MM SHAFT

FDA Adverse Event
Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·September 27, 2021

BARD

FDA Adverse Event
Injury ·BARD VASCULAR ACCESS·Product code FOS·March 14, 1997

ESOPHYX2 - LINK DESIGN - SHORT

FDA Adverse Event
Injury ·REDMOND·Product code ODE·July 19, 2011

COOK

FDA Adverse Event
Injury ·COOK·Product code FCL·June 19, 2014

OLYMPUS VIDEO UPPER ENDOSCOPE

FDA Adverse Event
Injury ·OLYMPUS AMERICA·Product code KOG·June 21, 2006

OLYMPUS COLONSCOPE

FDA Adverse Event
Injury ·OLYMPUS CORPORATION·Product code FDF·January 3, 1996

ILET BIONIC PANCREAS

FDA Adverse Event
Malfunction ·BETA BIONICS INC.·Product code QFG·December 11, 2025

MITYVAC

FDA Adverse Event
Malfunction ·PRISM HEALTH CARE·Product code HDB·November 28, 2003

TRUEMETRIX

FDA Adverse Event
Malfunction ·TRIVIDIA HEALTH, INC.·Product code NBW·September 19, 2019

MINI ONE® BALLOON BUTTON

FDA Adverse Event
Malfunction ·APPLIED MEDICAL TECHNOLOGY, INC.·Product code KNT·July 15, 2025

ORBERA INTRAGASTRIC BALLOON SYSTEM

FDA Adverse Event
Injury ·APOLLO ENDOSURGERY, INC.·Product code LTI·January 4, 2017