Z-2857-2018 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 Classic, Dual-Detector (Stitching Patient Support) 712052

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