ProxiDiagnost R90 1.0 and 1.1 multi-functional general R/F system, Model Numbers 706100 and 706110
Reported: April 19, 2023 Initiated: October 21, 2021 #Z-1356-2023
Product Description
ProxiDiagnost R90 1.0 and 1.1 multi-functional general R/F system, Model Numbers 706100 and 706110
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.
Details
- Recalling Firm
- Philips North America Llc
- Units Affected
- 243 units
- Distribution
- US Nationwide. Global Distribution.
- Location
- Cambridge, MA
Frequently Asked Questions
What product was recalled? ▼
ProxiDiagnost R90 1.0 and 1.1 multi-functional general R/F system, Model Numbers 706100 and 706110. Recalled by Philips North America Llc. Units affected: 243 units.
Why was this product recalled? ▼
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.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on April 19, 2023. Severity: Moderate. Recall number: Z-1356-2023.
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