FDA Device recall Z-1356-2023
ProxiDiagnost R90 1.0 and 1.1 multi-functional general R/F system, Model Numbers 706100 and 706110
- FDA Device
- Class II
- ongoing
- Published 2023-04-19
On 2023-04-19 the FDA classified a Class II recall of ProxiDiagnost R90 1.0 and 1.1 multi-functional general R/F system, Model Numbers 706100 and 706110 by Philips North America, citing if the system experiences an overvoltage / power surge it can cause a short circuit condition within the Main- cabinet. If this issue occurs, the user may experience an electrical….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1356-2023 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2021-10-21 |
| Published | 2023-04-19 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Philips North America |
| Distribution | US |
Product
ProxiDiagnost R90 1.0 and 1.1 multi-functional general R/F system, Model Numbers 706100 and 706110
Reason
If the system experiences an overvoltage / power surge it can cause a short circuit condition within the Main- cabinet. If this issue occurs, the user may experience an electrical fire within the cabinet, see or smell smoke emitting from the cabinet, or hear a popping sound coming from the cabinet.
Identifiers
| code_info | GTIN: (01)00884838085619 (Model 706100), (01)00884838103221 (Model 709031); Serial Numbers: 597241 10000000 10000001 10…GTIN: (01)00884838085619 (Model 706100), (01)00884838103221 (Model 709031); Serial Numbers: 597241 10000000 10000001 10000004 10000005 10000006 10000008 10000009 10000010 10000011 10000012 10000013 10000014 10000015 10000016 10000017 10000018 10000019 10000020 10000021 10000022 10000023 10000024 10000025 10000026 10000027 10000028 10000030 10000031 10000032 10000033 10000034 10000035 10000036 10000037 10000039 10000040 10000041 10000042 10000043 10000044 10000045 10000046 10000047 10000048 10000049 10000050 10000051 10000052 10000053 10000054 10000055 10001013 10001014 10001015 10001017 10001018 10001019 10001020 10001021 10001022 10001023 10001024 10001025 10001026 10001027 10001028 10001029 10001030 10001031 10001032 10001033 10001034 10001035 10001036 10001037 10001038 10001039 10001040 10001041 10001042 10001043 10001044 10001046 10001047 10001048 10001049 10001050 10001051 10001053 10001054 10001059 18000001 20000022 20000026 20000034 20000044 20000045 20000046 20000051 20000052 2 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1356-2023%22
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