Philips North America Llc
3000 Minuteman Rd, ANDOVER, MA, US
Registered product codes
39 product codes
Recent MDR events
21,177 on file
- Heart Start XLJul 31, 2026Malfunction3030677-2026-100819
- Heart Start XLJul 31, 2026Malfunction3030677-2026-100818
- HeartStartJul 31, 2026Malfunction3030677-2026-100817
- HeartStartJul 31, 2026Malfunction3030677-2026-100821
- PHILIPS HeartStart FRxJul 31, 2026Malfunction3030677-2026-100822
- PHILIPS HeartStart FRxJul 30, 2026Malfunction3030677-2026-100813
- HeartStartJul 30, 2026Malfunction3030677-2026-100814
- HeartStartJul 30, 2026Malfunction3030677-2026-100815
- HeartStartJul 30, 2026Malfunction3030677-2026-100816
- PHILIPS HeartStart FRxJul 29, 2026Malfunction3030677-2026-100812
Recalls
406 on file
- Open, ClassifiedAug 14, 2026
Device will intermittently provide inaccurate data related to native heart rate.
View FDA record ↗ - Open, ClassifiedAug 14, 2026
Device will intermittently provide inaccurate data related to native heart rate.
View FDA record ↗ - Open, ClassifiedJun 24, 2026
Potential for device reset to default "NEW_DEVICE" state, which may lead to a to loss of device configuration and the equipment label, resulting in a failure to reconnect to the PIC iX central monitoring system.
View FDA record ↗ - Open, ClassifiedJun 22, 2026
Monitor has incorrect assembly of the speaker connector which can cause device cables to be pulled out of the housing and increase the risk of intermittent or permanent loss of speaker output.
View FDA record ↗ - Open, ClassifiedJun 22, 2026
Monitor has incorrect assembly of the speaker connector which can cause device cables to be pulled out of the housing and increase the risk of intermittent or permanent loss of speaker output.
View FDA record ↗ - Open, ClassifiedJun 5, 2026
System was delivered without the required Seismic kit for Wall Stand VS2, which is designed to prevent damage and ensure stability of the Wall Stand VS2 during seismic events.
View FDA record ↗ - Open, ClassifiedFeb 6, 2026
As part of the CT systems sub assembly, thirty-two (32) fasteners are used to attach the rotor to the bearing within the gantry. One or more of these fasteners may not be torqued to specification. If multiple fasteners are not torqued to specification, the rotor or rotor parts may become unsecured or displaced. While there has been no reported or observed event of expelled parts during gantry rotation, unsecured rotor parts may potentially be expelled.
View FDA record ↗ - Open, ClassifiedFeb 6, 2026
As part of the CT systems sub assembly, thirty-two (32) fasteners are used to attach the rotor to the bearing within the gantry. One or more of these fasteners may not be torqued to specification. If multiple fasteners are not torqued to specification, the rotor or rotor parts may become unsecured or displaced. While there has been no reported or observed event of expelled parts during gantry rotation, unsecured rotor parts may potentially be expelled.
View FDA record ↗ - Open, ClassifiedFeb 6, 2026
As part of the CT systems sub assembly, thirty-two (32) fasteners are used to attach the rotor to the bearing within the gantry. One or more of these fasteners may not be torqued to specification. If multiple fasteners are not torqued to specification, the rotor or rotor parts may become unsecured or displaced. While there has been no reported or observed event of expelled parts during gantry rotation, unsecured rotor parts may potentially be expelled.
View FDA record ↗ - Open, ClassifiedFeb 6, 2026
As part of the CT systems sub assembly, thirty-two (32) fasteners are used to attach the rotor to the bearing within the gantry. One or more of these fasteners may not be torqued to specification. If multiple fasteners are not torqued to specification, the rotor or rotor parts may become unsecured or displaced. While there has been no reported or observed event of expelled parts during gantry rotation, unsecured rotor parts may potentially be expelled.
View FDA record ↗
Compliance history
Matched by FEI 1218950.
FDA inspections
0 on file
No inspections on file for this FEI number.
Inspection citations
0 on file
No citations on file for this FEI number.
Compliance actions
0 on file
No warning letters or injunctions on file for this FEI number.
Import refusals
1 on file
Top refusal reasons
Compare to industry ↗- Division of West Coast Imports (DWCI)Oct 25, 2024
74NSA \ OVER-THE-COUNTER AUTOMATED EXTERNAL DEFIBRILLATOR