FDA Device recall Z-2856-2018
DigitalDiagnost Classic 1.x Upgrades (Stitching Patient Support) 712081
- FDA Device
- Class II
- terminated
- Published 2018-08-29
On 2018-08-29 the FDA classified a Class II recall of DigitalDiagnost Classic 1.x Upgrades (Stitching Patient Support) 712081 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-2856-2018 |
| 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 1.x Upgrades (Stitching Patient Support) 712081
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: 456897/SN10000166 402837/SN0802410 2010345 410774/SN0802694 |
|---|
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-2856-2018%22
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