FDA Device recall Z-2862-2018
DigitalDiagnost Release 3.1 (Stitching Patient Support) 712026
- FDA Device
- Class II
- terminated
- Published 2018-08-29
On 2018-08-29 the FDA classified a Class II recall of DigitalDiagnost Release 3.1 (Stitching Patient Support) 712026 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-2862-2018 |
| 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 Release 3.1 (Stitching Patient Support) 712026
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: SN14000256 SN14000250 SN15000024 SN14000170 SN14000052 SN14000224 SN15000039 SN14000144 SN140…Serial Numbers: SN14000256 SN14000250 SN15000024 SN14000170 SN14000052 SN14000224 SN15000039 SN14000144 SN14000253 SN14000239 SN14000186 SN14000075 SN14000193 SN14000254 SN15000001 SN14000089 SN14000223 SN14000267 SN14000238 SN14000164 SN14000165 SN14000200 SN14000005 SN14000040 SN15000015 SN15000029 SN14000120 |
|---|
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-2862-2018%22
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