CombiDiagnost R90 1.0 and 1.1 multi-functional general R/F system, Model Numbers 709030 and 709031
Check against the official notice below — it lists the full affected range.
Philips North America is recalling 512 units of CombiDiagnost R90 1.0 and 1.1 multi-functional general R/F systems (Model Numbers 709030 and 709031) distributed nationwide and globally. If these systems experience an overvoltage or power surge, a short circuit condition can occur within the main cabinet, potentially causing an electrical fire, visible or detectable smoke, or a popping sound from the cabinet.
The recall affects specific serial numbers associated with each model. The source document does not specify what remedy affected consumers should take.
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: 512 units Lot/code info: GTIN: (01)00884838076747 (Model 709030), (01)00884838101456 (Model 709031; Serial Numbers: 10000000 10000001 10000002 10000003 10000004 10000006 10000007 10000010 10000011 10000012 10000013 10000014 10000015 10000016 10000019 10000020 10000021 10000022 10000023 10000024 10000025 10000026 10000027 10000029 10000030 10000031 10000032 10000034 10000035 10000036 10000037 10000038 10000040 10000041 10000042 10000043 10000044 10000045 10000046 10000047 10000048 10000049 10000050 10000051 10000052 10000053 10000054 10000055 10000056 10000057 10000058 10000060 10000061 10000063 10000064 10000065 10000066 10000067 10000068 10000069 10000070 10000071 10000072 10000073 10000075 10000076 10000078 10000079 10000080 10000081 10000082 10000083 10000087 10000089 10000090 10000092 10000093 10000094 10000095 10000096 10000097 10000099 10000100 10000102 10000103 10000104 10000107 10000108 10000109 10000111 10000112 10000114 10000115 10000116 10000117 10000118 10000119 10000121 10000122 10000124 10000125 10000126 10000127 10000130 10000131 10000133 10000134 10000135 10000136 10000137 10000138 10000139 10000140 10000144 10000145 10000149 10000151 10000152 10000156 10000165 10000166 10000168 10000169 10000170 10000171 10000174 10000176 10000178 10000179 10000180 10000184 10000185 10000186 10000187 10000188 10000189 10000190 10000191 10000194 10000198 10000199 10000202 10001000 10001001 10001010 10001070 10001071 10001072 10001073 10001074 10001075 10001076 10001078 10001079 10001080 10001081 10001
Official record: FDA (Device enforcement) ↗
Republished from the official source above; details can change — the source record controls.