Philips Medical Systems Gmbh, DMC: Medical Device Recall in 2018 - (Recall #: Z-2857-2018)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

Product Description:

DigitalDiagnost Classic, Dual-Detector (Stitching Patient Support) 712052

Product Classification:

Class II

Date Initiated: June 27, 2018

Date Posted: August 29, 2018

Recall Number: Z-2857-2018

Event ID: 80577

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.

Status: Terminated

Product Quantity:

Code Information:

Serial Numbers: 422102/SN0902020 435210/SN0902204 460471/SN1002019 433651/SN0902114 427610/SN0902108 470160/SN1102003 447013/SN1002008 445778/SN1002006 420208/SN0902019

Distribution Pattern:

US Nationwide; International to 66 countries

Voluntary or Mandated:

Voluntary: Firm initiated