Z-2857-2018 Class II Terminated
FDA device recall Z-2857-2018 was initiated by Philips Medical Systems Gmbh, DMC on Jun 27, 2018 and is designated Class II. 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. The recall status is terminated (terminated Apr 30, 2024).
Recall Details
- Product Type
- Devices
- Report Date
- Aug 29, 2018
- Initiation Date
- Jun 27, 2018
- Termination Date
- Apr 30, 2024
- Voluntary/Mandated
- Voluntary: Firm initiated
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
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-2857-2018
- openFDA file date
- Oct 23, 2026
- Loaded by RegDataLab
- Oct 26, 2026