Home / Brands / Philips Medical Systems Gmbh, DMC
Philips Medical Systems Gmbh, DMC Recalls
33 recalls on record · August 29, 2018 to September 8, 2021 · Medical Devices
Recalls by year
18
19
20
21
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
September 8, 2021Medical DevicesFDA
Philips Medical Systems Gmbh, DMC recalls CombiDiagnost R90 Software Version R1.0 and R1.1
Hazard: Philips has become aware of a software issue, where the kV and mA values are not locked immediately but change when the collimator shutter position is changed directly after the Lock-In command. This software issue leads to an over or under exposed image.
February 26, 2020Medical DevicesFDA
Philips Medical Systems Gmbh, DMC recalls CombiDiagnost PCF, Software v. 1.0.5, Product Code 709030 - Product Usage: Xray system, diagnostic, fluoroscopic, genera
Hazard: When using the Table Up/Down button, the system may experience Error 80, which locks the geometry in that specific state, requiring the intervention of a service Engineer. Additionally, the thermos switch, which handles power down of the unit in case of transformer overheating, was installed incorrectly at production.
February 26, 2020Medical DevicesFDA
Philips Medical Systems Gmbh, DMC recalls CombiDiagnost GCF, Software v. 1.0.5, Product Code 709030 - Product Usage: Xray system, diagnostic, fluoroscopic, genera
Hazard: When using the Table Up/Down button, the system may experience Error 80, which locks the geometry in that specific state, requiring the intervention of a service Engineer. Additionally, the thermos switch, which handles power down of the unit in case of transformer overheating, was installed incorrectly at production.
February 20, 2019Medical DevicesFDA
Philips Medical Systems Gmbh, DMC recalls Stationary Fluoroscopic X-ray System CombiDiagnost R90, Model 709030 Stationary Fluoroscopic X-ray System
Hazard: kV/mA lockin not functioning as specified which may result in the patient receiving an increased radiation dose.
October 31, 2018Medical DevicesFDA
Philips Medical Systems Gmbh, DMC recalls Philips DigitalDiagnost software 4.1.x and 4.2.x, A Stationary X-ray System Models: 712027, 712028, 712029, 712031, 712
Hazard: Stitching run on SkyPlate detector interrupted intermittently; Stitching with SkyPlate aborts after first image; System software CD contains wrong baseline
August 29, 2018Medical DevicesFDA
Philips Medical Systems Gmbh, DMC recalls EasyDiagnost Eleva DRF, Release 5 (Stitching Patient Support) 706050
Hazard: The hook does not securely hold the footplate in the vertical position. Therefore, the footplate can fall or swing down and injury operator or patient.
August 29, 2018Medical DevicesFDA
Philips Medical Systems Gmbh, DMC recalls EasyDiagnost Eleva DRF (Stitching Patient Support) 706032
Hazard: The hook does not securely hold the footplate in the vertical position. Therefore, the footplate can fall or swing down and injury operator or patient.
August 29, 2018Medical DevicesFDA
Philips Medical Systems Gmbh, DMC recalls DigitalDiagnost, Single-Detect (Stitching Patient Support) 712062
Hazard: The hook does not securely hold the footplate in the vertical position. Therefore, the footplate can fall or swing down and injury operator or patient.
August 29, 2018Medical DevicesFDA
Philips Medical Systems Gmbh, DMC recalls DigitalDiagnost, Dual-Detector (Stitching Patient Support) 712052
Hazard: The hook does not securely hold the footplate in the vertical position. Therefore, the footplate can fall or swing down and injury operator or patient.
August 29, 2018Medical DevicesFDA
Philips Medical Systems Gmbh, DMC recalls DigitalDiagnost Upgrades (Stitching Patient Support) 712083
Hazard: The hook does not securely hold the footplate in the vertical position. Therefore, the footplate can fall or swing down and injury operator or patient.
August 29, 2018Medical DevicesFDA
Philips Medical Systems Gmbh, DMC recalls DigitalDiagnost Single Detector (Stitching Patient Support) 712020
Hazard: The hook does not securely hold the footplate in the vertical position. Therefore, the footplate can fall or swing down and injury operator or patient.
August 29, 2018Medical DevicesFDA
Philips Medical Systems Gmbh, DMC recalls DigitalDiagnost Release 3.1 (Stitching Patient Support) 712026
Hazard: The hook does not securely hold the footplate in the vertical position. Therefore, the footplate can fall or swing down and injury operator or patient.
August 29, 2018Medical DevicesFDA
Philips Medical Systems Gmbh, DMC recalls DigitalDiagnost Release 3 (Stitching Patient Support) 712025
Hazard: The hook does not securely hold the footplate in the vertical position. Therefore, the footplate can fall or swing down and injury operator or patient.
August 29, 2018Medical DevicesFDA
Philips Medical Systems Gmbh, DMC recalls DigitalDiagnost Rel.4 Upgrades (Stitching Patient Support) 712084
Hazard: The hook does not securely hold the footplate in the vertical position. Therefore, the footplate can fall or swing down and injury operator or patient.
August 29, 2018Medical DevicesFDA
Philips Medical Systems Gmbh, DMC recalls DigitalDiagnost Dual Detector (Stitching Patient Support) 712022
Hazard: The hook does not securely hold the footplate in the vertical position. Therefore, the footplate can fall or swing down and injury operator or patient.
August 29, 2018Medical DevicesFDA
Philips Medical Systems Gmbh, DMC recalls DigitalDiagnost Dual Detector (Stitching Patient Support) 712022
Hazard: The hook does not securely hold the footplate in the vertical position. Therefore, the footplate can fall or swing down and injury operator or patient.
August 29, 2018Medical DevicesFDA
Philips Medical Systems Gmbh, DMC recalls DigitalDiagnost Classic, Dual-Detector (Stitching Patient Support) 712052
Hazard: The hook does not securely hold the footplate in the vertical position. Therefore, the footplate can fall or swing down and injury operator or patient.
August 29, 2018Medical DevicesFDA
Philips Medical Systems Gmbh, DMC recalls DigitalDiagnost Classic 1.x Upgrades (Stitching Patient Support) 712081
Hazard: The hook does not securely hold the footplate in the vertical position. Therefore, the footplate can fall or swing down and injury operator or patient.
August 29, 2018Medical DevicesFDA
Philips Medical Systems Gmbh, DMC recalls DigitalDiagnost 4.1 High Performance (Stitching Patient Support) 712031
Hazard: The hook does not securely hold the footplate in the vertical position. Therefore, the footplate can fall or swing down and injury operator or patient.
August 29, 2018Medical DevicesFDA
Philips Medical Systems Gmbh, DMC recalls DigitalDiagnost 4.1 Flex / Value (Stitching Patient Support) 712028
Hazard: The hook does not securely hold the footplate in the vertical position. Therefore, the footplate can fall or swing down and injury operator or patient.
August 29, 2018Medical DevicesFDA
Philips Medical Systems Gmbh, DMC recalls DigitalDiagnost 4.1 Chest / Emergency (Stitching Patient Support) 712029
Hazard: The hook does not securely hold the footplate in the vertical position. Therefore, the footplate can fall or swing down and injury operator or patient.
August 29, 2018Medical DevicesFDA
Philips Medical Systems Gmbh, DMC recalls DigitalDiagnost 4.1 (Stitching Patient Support) 712225
Hazard: The hook does not securely hold the footplate in the vertical position. Therefore, the footplate can fall or swing down and injury operator or patient.
August 29, 2018Medical DevicesFDA
Philips Medical Systems Gmbh, DMC recalls DigitalDiagnost 4 High Performance (Stitching Patient Support) 712027
Hazard: The hook does not securely hold the footplate in the vertical position. Therefore, the footplate can fall or swing down and injury operator or patient.
August 29, 2018Medical DevicesFDA
Philips Medical Systems Gmbh, DMC recalls DigitalDiagnost 4 Flex / Value (Stitching Patient Support) 712028
Hazard: The hook does not securely hold the footplate in the vertical position. Therefore, the footplate can fall or swing down and injury operator or patient.
August 29, 2018Medical DevicesFDA
Philips Medical Systems Gmbh, DMC recalls DigitalDiagnost 4 Chest / Emergency (Stitching Patient Support) 712029
Hazard: The hook does not securely hold the footplate in the vertical position. Therefore, the footplate can fall or swing down and injury operator or patient.
August 29, 2018Medical DevicesFDA
Philips Medical Systems Gmbh, DMC recalls DigitalDiagnost 2.x Upgrades (Stitching Patient Support) 712081
Hazard: The hook does not securely hold the footplate in the vertical position. Therefore, the footplate can fall or swing down and injury operator or patient.
August 29, 2018Medical DevicesFDA
Philips Medical Systems Gmbh, DMC recalls CombiDiagnost R90 (Stitching Patient Support) 709030
Hazard: The hook does not securely hold the footplate in the vertical position. Therefore, the footplate can fall or swing down and injury operator or patient.
August 29, 2018Medical DevicesFDA
Philips Medical Systems Gmbh, DMC recalls BuckyDiagnost Ceiling System (Stitching Patient Support) 704031
Hazard: The hook does not securely hold the footplate in the vertical position. Therefore, the footplate can fall or swing down and injury operator or patient.
August 29, 2018Medical DevicesFDA
Philips Medical Systems Gmbh, DMC recalls DigitalDiagnost Release 3.1 (Stitching Patient Support) 712026
Hazard: The hook does not securely hold the footplate in the vertical position. Therefore, the footplate can fall or swing down and injury operator or patient.
August 29, 2018Medical DevicesFDA
Philips Medical Systems Gmbh, DMC recalls DigitalDiagnost Release 3 (Stitching Patient Support) 712025
Hazard: The hook does not securely hold the footplate in the vertical position. Therefore, the footplate can fall or swing down and injury operator or patient.