DigitalDiagnost C90 Flex/Value/Chest/ER, used to acquire, process, store, display and export digital radiographic images.
Reported: November 15, 2023 Initiated: September 21, 2023 #Z-0275-2024
Product Description
DigitalDiagnost C90 Flex/Value/Chest/ER, used to acquire, process, store, display and export digital radiographic images.
Reason for Recall
Potential for units suspended on the ceiling to fail and fall.
Details
- Recalling Firm
- Philips North America Llc
- Units Affected
- 33 units
- Distribution
- Nationwide distribution.
- Location
- Cambridge, MA
Frequently Asked Questions
What product was recalled? ▼
DigitalDiagnost C90 Flex/Value/Chest/ER, used to acquire, process, store, display and export digital radiographic images.. Recalled by Philips North America Llc. Units affected: 33 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-0275-2024.
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