23 results · 112ms · Sources: EU EUDAMED, US FDA

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8.3MHZ PENCIL PROBE 7 FOOT ODU CONNECTOR

FDA Adverse Event
Injury ·PARKS MEDICAL ELECTRONICS, INC.·Product code JOP·June 24, 2025

NA

FDA Adverse Event
PARKS MEDICAL ELECTRONICS, INC.·Product code IYN·August 31, 2015

FLOWMETER, BLOOD, CARDIOVASCULAR

FDA Adverse Event
Malfunction ·PARKS MEDICAL ELECTRONICS, INC.·Product code DPW·October 5, 2017

FLO-LAB

FDA Adverse Event
Injury ·PARKS MEDICAL ELECTRONICS INC.·Product code MHX·April 24, 2012

NA

FDA Adverse Event
Malfunction ·PARKS MEDICAL ELECTRONICS, INC.·Product code MHX·December 31, 2009

DOPPLER MODEL 812

FDA Adverse Event
Malfunction ·PARKS MEDICAL ELECTRONICS, INC.·Product code DPW·August 27, 2025

FLO LAB

FDA Adverse Event
Other ·PARKS MEDICAL ELECTRONICS, INC·Product code DXN·April 7, 2006

1052

FDA Adverse Event
Other ·PARKS MEDICAL ELECTRONICS, INC.·Product code IYN·April 10, 2006

9.1MHZ PENCIL PROBE

FDA Adverse Event
Malfunction ·PARKS MEDICAL ELECTRONICS, INC.·Product code JOP·June 2, 2025

FLO-LAB

FDA Adverse Event
Malfunction ·PARKS MEDICAL ELECTRONICS, INC.·Product code MWI·May 11, 2017

DOPPLER PENCIL PROBE

FDA Adverse Event
Malfunction ·PARKS MEDICAL ELECTRONICS, INC·Product code IYN·March 3, 2015

FLO-LAB

FDA Adverse Event
Other ·PARKS MEDICAL ELECTRONICS, INC. (PMEI)·Product code MHX·January 15, 2013

MINIMED 770G US SYSTEM BLE CONNECT 3.0 MG/DL

FDA Adverse Event
Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·August 11, 2021

MINIMED 770G US SYSTEM BLE CONNECT 3.0 MG/DL

FDA Adverse Event
Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·August 24, 2021

MINIMED 770G US SYSTEM BLE CONNECT 3.0 MG/DL

FDA Adverse Event
Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·October 5, 2021

MINIMED 770G US SYSTEM BLE CONNECT 3.0 MG/DL

FDA Adverse Event
Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·September 15, 2021

PUMP MMT-1780KPK 670G PATHWAY BLACK MG

FDA Adverse Event
Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·June 18, 2021

UNKNOWN OPTEASE VENA CAVA FILTER

FDA Adverse Event
Injury ·CORDIS CORPORATION·Product code DTK·July 7, 2015

PUMP MMT-1780KPK 670G PATHWAY BLACK MG

FDA Adverse Event
Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·February 13, 2020

PUMP MMT-1780KPK 670G PATHWAY BLACK MG

FDA Adverse Event
Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·July 20, 2021