ProxiDiagnost N90, Radiography and Fluoroscopy (R/F) system
Reported: November 15, 2023 Initiated: September 21, 2023 #Z-0280-2024
Product Description
ProxiDiagnost N90, Radiography and Fluoroscopy (R/F) system
Reason for Recall
Potential for units suspended on the ceiling to fail and fall.
Details
- Recalling Firm
- Philips North America Llc
- Units Affected
- 101 units
- Distribution
- Nationwide distribution.
- Location
- Cambridge, MA
Frequently Asked Questions
What product was recalled? ▼
ProxiDiagnost N90, Radiography and Fluoroscopy (R/F) system. Recalled by Philips North America Llc. Units affected: 101 units.
Why was this product recalled? ▼
Potential for units suspended on the ceiling to fail and fall.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on November 15, 2023. Severity: Moderate. Recall number: Z-0280-2024.
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