ProxiDiagnost R90 1.0 and 1.1 multi-functional general R/F system, Model Numbers 706100 and 706110
Check against the official notice below — it lists the full affected range.
Philips North America LLC is recalling 243 units of the ProxiDiagnost R90 1.0 and 1.1 multi-functional general X-ray systems (Model Numbers 706100 and 706110) distributed nationwide and globally. If these systems experience an overvoltage or power surge, a short circuit condition can develop within the main cabinet, potentially causing an electrical fire, visible smoke, or a popping sound coming from the cabinet.
The recall affects specific serial numbers identified in this notice. The source does not specify a remedy for affected consumers.
Written by software from the official notice below. Not reviewed by a lawyer.
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.
Reason for recall: 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. Distribution: US Nationwide. Global Distribution. Quantity: 243 units Lot/code info: 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 20000054 20000055 20000061 20000062 20000063 20000064 20000065 20000066 20000067 20000068 20000069 20000070 20000071 20000072 20000073 20000074 20000077 20000078 20000079 20000081 20000082 20000083 20000085 20000086 20000089 721815121706 SN10001000 SN10001001 SN10001002 SN10001003 SN10001004 SN10001005 SN10001006 SN10001007 SN10001008 SN10001009 SN10001010 SN10001011 SN10001012 SN18000001 SN18000002 SN18000003 SN18000004 SN18000005 SN18000006 SN18000007 SN18000008 SN18000009 SN18000011 SN18000012
Official record: FDA (Device enforcement) ↗
Republished from the official source above; details can change — the source record controls.