3 results
·
11ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Open, Classified
×
LIFEPAK 35 ECG cable REF 11111-000041
FDA Recall
Open, Classified
·Physio-Control, Inc.·Product code DSA·January 21, 2025
LIFEPAK 20e REF 99507-000001 The AED mode is to be used only on patients in cardiopulmonary arrest.
FDA Recall
Open, Classified
·Physio-Control, Inc.·Product code MKJ·February 3, 2025
LIFEPAK 15 (LP15) Model/Catalog Numbers: o 97577-000101 o 99577-000046 o 99577-000055 o 99577-000061 o 99577-000076 o 99577-001250 o 99577-001255 o 99577-001256 o 99577-001368 o 99577-001955 o 99577-001956 o 99577-001957 o 99577-001958 o 99577-001962 LIFEPAK 15 intended use monitor/defibrillator.
FDA Recall
Open, Classified
·Physio-Control, Inc.·Product code MKJ·August 30, 2024