FDA Device recall Z-2857-2018
DigitalDiagnost Classic, Dual-Detector (Stitching Patient Support) 712052
- FDA Device
- Class II
- terminated
- Published 2018-08-29
On 2018-08-29 the FDA classified a Class II recall of DigitalDiagnost Classic, Dual-Detector (Stitching Patient Support) 712052 by Philips Medical Systems Dmc, citing 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.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2857-2018 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2018-06-27 |
| Published | 2018-08-29 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Philips Medical Systems Dmc |
| Distribution | US |
Product
DigitalDiagnost Classic, Dual-Detector (Stitching Patient Support) 712052
Reason
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.
Identifiers
| code_info | Serial Numbers: 422102/SN0902020 435210/SN0902204 460471/SN1002019 433651/SN0902114 427610/SN0902108 470160/SN11…Serial Numbers: 422102/SN0902020 435210/SN0902204 460471/SN1002019 433651/SN0902114 427610/SN0902108 470160/SN1102003 447013/SN1002008 445778/SN1002006 420208/SN0902019 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2857-2018%22
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