FDA Device recall Z-2854-2018
DigitalDiagnost 4.1 Flex / Value (Stitching Patient Support) 712028
- FDA Device
- Class II
- terminated
- Published 2018-08-29
On 2018-08-29 the FDA classified a Class II recall of DigitalDiagnost 4.1 Flex / Value (Stitching Patient Support) 712028 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-2854-2018 |
| 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 4.1 Flex / Value (Stitching Patient Support) 712028
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: SN16000197 SN15000288 SN16000234 SN16000008 SN15000304 SN15000283 SN15000174 SN15000225 SN160…Serial Numbers: SN16000197 SN15000288 SN16000234 SN16000008 SN15000304 SN15000283 SN15000174 SN15000225 SN16000124 SN16000023 550162 SN15000350 SN16000092 SN15000379 SN16000283 SN16000104 SN15000173 |
|---|
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-2854-2018%22
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