Home / Recalls / Philips Medical Systems Gmbh, DMC / Z-2843-2018

Z-2843-2018 Class II Terminated

Recalled by Philips Medical Systems Gmbh, DMC — Hamburg

Recall Details

Product Type
Devices
Report Date
August 29, 2018
Initiation Date
June 27, 2018
Termination Date
April 30, 2024
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity

Product Description

DigitalDiagnost 4.1 High Performance (Stitching Patient Support) 712031

Reason for Recall

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.

Distribution Pattern

US Nationwide; International to 66 countries

Code Information

Serial Numbers: SN15000196 SN15000180 SN15000282 SN15000281 SN15000192 SN15000189

Other recalls by Philips Medical Systems Gmbh, DMC

  • Z-2357-2021 Class II — CombiDiagnost R90 Software Version R1.0 and R1.1 (July 22, 2020)
  • Z-1328-2020 Class II — CombiDiagnost GCF, Software v. 1.0.5, Product Code 709030 - Product Usage: Xray (December 19, 2019)
  • Z-1329-2020 Class II — CombiDiagnost PCF, Software v. 1.0.5, Product Code 709030 - Product Usage: Xray (December 19, 2019)
  • Z-0612-2019 Class II — Stationary Fluoroscopic X-ray System CombiDiagnost R90, Model 709030 Stationa (November 7, 2018)
  • Z-0239-2019 Class II — Philips DigitalDiagnost software 4.1.x and 4.2.x, A Stationary X-ray System Mod (September 19, 2018)
  • Z-2863-2018 Class II — DigitalDiagnost Single Detector (Stitching Patient Support) 712020 (June 27, 2018)
  • Z-2867-2018 Class II — EasyDiagnost Eleva DRF (Stitching Patient Support) 706032 (June 27, 2018)
  • Z-2862-2018 Class II — DigitalDiagnost Release 3.1 (Stitching Patient Support) 712026 (June 27, 2018)
  • Z-2855-2018 Class II — DigitalDiagnost 4.1 High Performance (Stitching Patient Support) 712031 (June 27, 2018)
  • Z-2849-2018 Class II — DigitalDiagnost 4 Chest / Emergency (Stitching Patient Support) 712029 (June 27, 2018)