Medical Device Recalls
-
1 to 7 of 7 Results
510(K) Number: K142430 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
LIFEPAK 15 MONITOR/DEFIBRILLATOR that was either manufactured with or received an upgrade kit that c... | 2 | 01/16/2020 | Physio-Control, Inc. |
LIFEPAK 15 MONITOR/DEFIBRILLATOR service kits | 2 | 01/16/2020 | Physio-Control, Inc. |
LIFEPAK 15 Monitor/Defibrillator with End-Tidal CO2 option. Intended for use by trained medic... | 2 | 02/07/2017 | Physio-Control, Inc. |
LIFEPAK15 monitor/defibrillator with End-Tidal C02 (EtC02) feature installed. Part numbers: V... | 2 | 06/15/2016 | Physio-Control, Inc. |
LIFEPAK 15 Monitor/Defibrillator Product Usage: The LIFEPAK(R) 15 Monitor/defibrillator (LP15) i... | 1 | 02/26/2019 | Physio-Control Inc |
LIFEPAK 15 Monitor/Defibrillator service kits Product Usage: The LIFEPAK(R) 15 Monitor/defibrill... | 1 | 02/26/2019 | Physio-Control Inc |
LIFEPAK 15 Monitor, Automated External Defibrillator (AED), Manual mode monitoring and therapy funct... | 1 | 02/11/2017 | Physio-Control, Inc. |
-